Riboflavin Missence Mutation Data


Gene SymbolChromosomeStartEndrs IDStrandNCBI refObservedClassFunctionSubmitter CountSubmitterFrequency CountAllele Frequency
ACOX1chr177394445673944457rs35105560+CC/Tsinglemissense1APPLERA_GI,20.987179
ACOX1chr177394449573944496rs35629489+GA/Gsinglemissense91000GENOMES,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,SEATTLESEQ,TISHKOFF,20.010675
ACOX1chr177394953973949540rs1135640-GC/Gsinglemissense301000GENOMES,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,CORNELL,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,LEE,MGC_GENOME_DIFF,NHLBI-ESP,PERLEGEN,PJP,SEATTLESEQ,SEQUENOM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,WUGSC_SSAHASNP,20.476613
ACOX1chr177396983473969835rs3744032+CC/Tsingleintron,missense151000GENOMES,AFFY,CLINSEQ_SNP,COMPLETE_GENOMICS,EXOME_CHIP,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,SEATTLESEQ,SSMP,TISHKOFF,YUSUKE,20.939938
FDXRchr177286065272860653rs34038065-GC/TsinglencRNA,missense101000GENOMES,CLINSEQ_SNP,CORNELL,EGP_SNPS,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,SSMP,TISHKOFF,20.976671
FDXRchr177286105672861057rs35102176-GC/Gsingleintron,missense71000GENOMES,BUSHMAN,EGP_SNPS,EXOME_CHIP,ILLUMINA,NHLBI-ESP,TISHKOFF,20.983936
FDXRchr177286259272862593rs690514-CA/Gsingleintron,ncRNA,missense201000GENOMES,ABI,BGI,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CORNELL,EGP_SNPS,EXOME_CHIP,GMI,HGBASE,ILLUMINA,LEE,NHLBI-ESP,SC_JCM,SEATTLESEQ,SSMP,TISHKOFF,WIAF-CSNP,YUSUKE,20.186529
FDXRchr177286302972863030rs1688149-TA/Gsingleintron,missense121000GENOMES,ABI,BGI,BUSHMAN,COMPLETE_GENOMICS,EGP_SNPS,GMI,HGSV,NHLBI-ESP,SC_JCM,SSMP,TISHKOFF,20.781250
PNPOchr174602206446022065rs17679445+GA/Gsinglemissense91000GENOMES,AFFY,CLINSEQ_SNP,CORNELL,EXOME_CHIP,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,20.044352
SLC52A1chr1749368974936898rs2304445-CA/Gsinglemissense171000GENOMES,ABI,BGI,BUSHMAN,CLINSEQ_SNP,ENSEMBL,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PJP,SEATTLESEQ,SSMP,TISHKOFF,YUSUKE,20.217189
SLC52A1chr1749369714936972rs346821+GA/Gsinglemissense251000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KWOK,MGC_GENOME_DIFF,NHLBI-ESP,PJP,SC_JCM,SEATTLESEQ,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.643869
SLC52A1chr1749375744937575rs346822-TA/Gsinglemissense271000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KWOK,MGC_GENOME_DIFF,NHLBI-ESP,PERLEGEN,PJP,SC_JCM,SEATTLESEQ,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.058377
NDUFV2chr1891178669117867rs906807-TA/Gsinglemissense271000GENOMES,ABI,AFFY,APPLERA_GI,BCMHGSC_JDW,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HGBASE,HUMANGENOME_JCVI,ILLUMINA,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,PERLEGEN,PJP,RIKENSNPRC,SEATTLESEQ,SI_EXO,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.209829
NDUFV2chr1891226109122611rs72935225+TC/Tsinglemissense6BL,BUSHMAN,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,SEATTLESEQ,20.091670
ACP5chr191168713111687132rs2229532-CA/Gsinglemissense121000GENOMES,APPLERA_GI,CLINSEQ_SNP,COMPLETE_GENOMICS,EXOME_CHIP,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,SEATTLESEQ,TISHKOFF,WICVAR,20.038484
ACP5chr191168719411687195rs2229531-CA/Gsinglemissense121000GENOMES,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,SI_EXO,SSMP,WICVAR,YUSUKE,20.075470
ACP5chr191168735011687351rs2305799+CC/Tsinglemissense131000GENOMES,AFFY,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,PERLEGEN,SI_EXO,SSMP,TISHKOFF,YUSUKE,20.907794
ETFBchr195185028951850290rs1130426-GA/C/G/Tsinglemissense261000GENOMES,AFFY,APPLERA_GI,BL,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,EXOME_CHIP,GMI,HGBASE,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,LEE,NHLBI-ESP,PJP,SEATTLESEQ,SEQUENOM,SSAHASNP,SSMP,TISHKOFF,WICVAR,WI_SSAHASNP,40.000103
ETFBchr195185773751857738rs79338777+GA/Gsingleintron,missense91000GENOMES,CLINSEQ_SNP,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,SEATTLESEQ,SSMP,TISHKOFF,20.063373
GCDHchr191301051513010516rs113720193+GA/Gsingleintron,ncRNA,missense,untranslated-371000GENOMES,BUSHMAN,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,TISHKOFF,20.016030
GCDHchr191301051913010520rs8012+AA/Gsingleintron,ncRNA,missense,untranslated-3251000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,LEE,NHLBI-ESP,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,30.293339
ACP1chr2264984264985rs11691572+GG/Tsinglenear-gene-5,ncRNA,missense91000GENOMES,ABI,AFFY,BUSHMAN,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,ILLUMINA,NHLBI-ESP,20.989735
ACP1chr2272202272203rs11553746+CC/Tsinglecoding-synon,intron,ncRNA,missense191000GENOMES,APPLERA_GI,BCM-HGSC-SUB,BCMHGSC_JDW,BL,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,SEATTLESEQ,SSMP,TISHKOFF,20.738443
ACP1chr2277002277003rs79716074+AA/GsinglencRNA,missense191000GENOMES,BCM-HGSC-SUB,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,EXOME_CHIP,GMI,HGSV,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,OMIM-CURATED-RECORDS,PJP,SEATTLESEQ,SEQUENOM,SSMP,TISHKOFF,WI_SSAHASNP,20.725060
ACP1chr2277236277237rs35569198-CA/GsinglencRNA,missense3APPLERA_GI,ILLUMINA,PERLEGEN,20.026316
D2HGDHchr2242674681242674682rs4675887-CC/Gsinglemissense41000GENOMES,EXOME_CHIP,SSMP,WI_SSAHASNP,20.037190
D2HGDHchr2242674802242674803rs77940364+GA/Gsinglemissense81000GENOMES,BGI,BL,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,SSMP,20.214534
D2HGDHchr2242690674242690675rs1106639+GA/Gsinglemissense121000GENOMES,APPLERA_GI,BGI,BL,COMPLETE_GENOMICS,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,SSMP,TISHKOFF,TSC-CSHL,20.258387
D2HGDHchr2242690728242690729rs144668507+CC/Tsinglemissense51000GENOMES,EXOME_CHIP,ILLUMINA,NHLBI-ESP,TISHKOFF,20.976779
D2HGDHchr2242690744242690745rs1105273+CC/Tsinglemissense111000GENOMES,APPLERA_GI,BUSHMAN,COMPLETE_GENOMICS,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,SSMP,TISHKOFF,TSC-CSHL,20.817032
XDHchr23156057131560572rs45564939-GC/Tsinglemissense61000GENOMES,CLINSEQ_SNP,EGP_SNPS,EXOME_CHIP,ILLUMINA,NHLBI-ESP,20.989163
XDHchr23156061631560617rs181743036+CC/Tsinglemissense11000GENOMES,20.975666
XDHchr23156965931569660rs45547640-TA/Csinglemissense51000GENOMES,EGP_SNPS,EXOME_CHIP,GMI,ILLUMINA,20.989380
XDHchr23157039231570393rs45619033-CC/Gsinglemissense81000GENOMES,CORNELL,EGP_SNPS,EXOME_CHIP,ILLUMINA,NHLBI-ESP,PHARMGKB_AB_DME,SNP500CANCER,20.012859
XDHchr23159091631590917rs17011368+TC/Tsinglemissense181000GENOMES,AFFY,APPLERA_GI,CLINSEQ_SNP,EGP_SNPS,EXOME_CHIP,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PHARMGKB_AB_DME,SEATTLESEQ,SI_EXO,SNP500CANCER,SSMP,TISHKOFF,20.058112
XDHchr23159326431593265rs17323225+TC/Tsinglemissense131000GENOMES,AFFY,APPLERA_GI,CLINSEQ_SNP,EGP_SNPS,EXOME_CHIP,GMI,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PHARMGKB_AB_DME,SSMP,20.022365
XDHchr23159514831595149rs61731081+CC/Tsinglemissense2AFFY_DM3_1,CORNELL,20.985714
XDHchr23160279031602791rs34929837-TA/Tsinglemissense101000GENOMES,APPLERA_GI,CLINSEQ_SNP,EGP_SNPS,EXOME_CHIP,ILLUMINA,NHLBI-ESP,PERLEGEN,PHARMGKB_AB_DME,SNP500CANCER,20.981743
XDHchr23161114231611143rs45523133-CA/Gsinglemissense101000GENOMES,BUSHMAN,CLINSEQ_SNP,EGP_SNPS,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SEATTLESEQ,SSMP,TISHKOFF,20.028118
SLC52A3chr20744166744167rs76947760+AA/Tsinglemissense61000GENOMES,BUSHMAN,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SEATTLESEQ,20.979486
SLC52A3chr20744307744308rs3746802+TC/Tsinglemissense221000GENOMES,ABI,AFFY,BCM-HGSC-SUB,CLINSEQ_SNP,COMPLETE_GENOMICS,CORNELL,ENSEMBL,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,MGC_GENOME_DIFF,NHLBI-ESP,PERLEGEN,PJP,SEATTLESEQ,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,20.098919
SLC52A3chr20744381744382rs3746803+GA/Gsinglemissense231000GENOMES,ABI,AFFY,APPLERA_GI,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,MGC_GENOME_DIFF,NHLBI-ESP,PERLEGEN,PJP,SEATTLESEQ,SI_EXO,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,30.096882
SLC52A3chr20744414744415rs3746804+GA/Gsinglemissense251000GENOMES,ABI,AFFY,APPLERA_GI,BCM-HGSC-SUB,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,MGC_GENOME_DIFF,NHLBI-ESP,PERLEGEN,PJP,SEATTLESEQ,SI_EXO,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,20.205550
SLC52A3chr20745897745898rs6054614+TC/Tsinglemissense101000GENOMES,BUSHMAN,EXOME_CHIP,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,SC_SNP,SEATTLESEQ,TISHKOFF,20.013094
SLC52A3chr20746196746197rs35655964-GC/Gsinglemissense91000GENOMES,APPLERA_GI,COMPLETE_GENOMICS,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,SSMP,TISHKOFF,20.942274
CYB5R3chr224302364743023648rs61743717+CA/Csinglemissense1CORNELL,20.013513
CYB5R3chr224302427043024271rs1800457-GC/Gsinglemissense151000GENOMES,ABI,CLINSEQ_SNP,CORNELL,CSHL-HAPMAP,EGP_SNPS,EXOME_CHIP,HGBASE,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,OMIM-CURATED-RECORDS,PERLEGEN,SEATTLESEQ,TISHKOFF,20.907836
CYB5R3chr224304043343040434rs8190407-GC/Gsingleintron,missense91000GENOMES,AFFY,EGP_SNPS,EXOME_CHIP,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,TISHKOFF,20.978081
PRODHchr221890100318901004rs450046+CC/Tsinglemissense331000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,CANCER-GENOME,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGBASE,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,LEE,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,PERLEGEN,PJP,SC_JCM,SC_SNP,SEATTLESEQ,SEQUENOM,SI_EXO,SSMP,TISHKOFF,WI_SSAHASNP,20.101300
PRODHchr221890584118905842rs2870983+CC/Tsinglemissense71000GENOMES,CLINSEQ_SNP,EXOME_CHIP,NHLBI-ESP,SSMP,TISHKOFF,TSC-CSHL,20.953161
PRODHchr221890589818905899rs3970559+GA/Gsinglemissense101000GENOMES,BCM_SSAHASNP,CLINSEQ_SNP,EXOME_CHIP,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,SC_SNP,SSMP,TSC-CSHL,20.011183
PRODHchr221890596318905964rs2904552+CC/Tsinglemissense131000GENOMES,ABI,CLINSEQ_SNP,ENSEMBL,EXOME_CHIP,HUMANGENOME_JCVI,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,PJP,SSAHASNP,TISHKOFF,TSC-CSHL,20.929709
PRODHchr221890597618905977rs2238731+CC/Tsinglemissense91000GENOMES,CLINSEQ_SNP,EXOME_CHIP,NHLBI-ESP,SC_SNP,SI_EXO,SSMP,TISHKOFF,YUSUKE,20.955779
PRODHchr221891035418910355rs5747933+GG/Tsinglemissense81000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SC_SNP,SEATTLESEQ,SSMP,20.950928
PRODHchr221891267618912677rs11913840+CC/Tsinglemissense61000GENOMES,CLINSEQ_SNP,CSHL-HAPMAP,EXOME_CHIP,NHLBI-ESP,SSMP,20.945209
PRODHchr221892362818923629rs146648839+CC/Tsingleintron,missense31000GENOMES,EXOME_CHIP,NHLBI-ESP,20.960514
PRODHchr221892371218923713rs3815655+GA/Gsingleintron,missense61000GENOMES,COMPLETE_GENOMICS,EXOME_CHIP,HGSV,SSMP,YUSUKE,20.125229
PRODHchr221892374418923745rs2008720-GA/Csingleintron,missense161000GENOMES,ABI,BCM-HGSC-SUB,BGI,CSHL-HAPMAP,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,PJP,SEQUENOM,SSAHASNP,SSMP,TSC-CSHL,WI_SSAHASNP,YUSUKE,20.543462
TXNRD2chr221986821719868218rs1139793+AA/Gsinglemissense311000GENOMES,AFFY,AFFY_GWHS,APPLERA_GI,BCMHGSC_JDW,BGI,BL,BUSHMAN,CGAP-GAI,CGM_KYOTO,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGBASE,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,LEE,NHLBI-ESP,PERLEGEN,PJP,SC_SNP,SEATTLESEQ,SSAHASNP,SSMP,TISHKOFF,YUSUKE,50.247231
TXNRD2chr221987089719870898rs61736941+GA/Gsinglemissense2CORNELL,NHLBI-ESP,20.013513
TXNRD2chr221988298319882984rs5992495+TG/Tsinglemissense201000GENOMES,ABI,AFFY,BUSHMAN,CLINSEQ_SNP,CORNELL,ENSEMBL,EXOME_CHIP,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PJP,SC_SNP,SEATTLESEQ,SSMP,TISHKOFF,20.232925
TXNRD2chr221990328919903290rs61736929+CC/Gsinglemissense91000GENOMES,CLINSEQ_SNP,CORNELL,EXOME_CHIP,GOLDSTEINLAB,ILLUMINA,NHLBI-ESP,SEATTLESEQ,TISHKOFF,20.963597
TXNRD2chr221990709819907099rs5748469+CA/Csinglemissense201000GENOMES,BCM-HGSC-SUB,BGI,BL,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,CORNELL,EXOME_CHIP,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,SC_SNP,SEATTLESEQ,SSMP,TISHKOFF,20.463202
ACAD9chr3128622921128622922rs115532916+GA/C/GsinglencRNA,missense61000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,OMIM-CURATED-RECORDS,20.013100
ACAD9chr3128627886128627887rs4494951+GA/GsinglencRNA,missense111000GENOMES,ABI,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,DEVINE_LAB,EXOME_CHIP,ILLUMINA,NHLBI-ESP,PERLEGEN,SC_JCM,20.011064
ACAD9chr3128634036128634037rs113633667+CC/Tsinglemissense41000GENOMES,CLINSEQ_SNP,COMPLETE_GENOMICS,ILLUMINA,20.989467
ETFDHchr4159601675159601676rs11559290+CC/Tsinglemissense261000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,CORNELL,ENSEMBL,EXOME_CHIP,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,MGC_GENOME_DIFF,NHLBI-ESP,PERLEGEN,PJP,SEATTLESEQ,SSAHASNP,SSMP,TISHKOFF,20.323065
MTRRchr578668207866821rs16879259+TC/Tsingleintron,missense131000GENOMES,AFFY,BUSHMAN,CLINSEQ_SNP,EXOME_CHIP,GMI,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,PERLEGEN,SEATTLESEQ,SSMP,TISHKOFF,20.065686
MTRRchr578680297868030rs2966952+TC/Tsingleintron,near-gene-5,missense271000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PJP,SC_JCM,SEATTLESEQ,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,20.834742
MTRRchr578709727870973rs1801394+AA/Gsinglenear-gene-5,missense291000GENOMES,ABI,AFFY,APPLERA_GI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HGBASE,HUMANGENOME_JCVI,ILLUMINA,KYUGEN,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,PHARMGKB_PPII,PJP,SEATTLESEQ,SI_EXO,SNP500CANCER,SSMP,TISHKOFF,YUSUKE,20.572342
MTRRchr578781787878179rs1532268-CA/Gsinglemissense271000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CORNELL,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,PJP,SEATTLESEQ,SNP500CANCER,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,YUSUKE,20.295599
MTRRchr578784237878424rs2303080+TA/Tsinglemissense131000GENOMES,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,HGSV,ILLUMINA,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,PJP,SEATTLESEQ,SSMP,YUSUKE,20.030610
MTRRchr578859067885907rs10064631+CC/Gsinglemissense121000GENOMES,BUSHMAN,EXOME_CHIP,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,SEATTLESEQ,TISHKOFF,WI_SSAHASNP,20.947887
MTRRchr578859587885959rs162036+AA/Gsinglemissense231000GENOMES,ABI,AFFY,BCM_SSAHASNP,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,KWOK,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,PJP,SC_JCM,SEATTLESEQ,SSMP,TISHKOFF,20.774035
MTRRchr578893037889304rs2287780+CC/Tsinglemissense161000GENOMES,APPLERA_GI,BUSHMAN,CLINSEQ_SNP,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,SEATTLESEQ,SI_EXO,SNP500CANCER,SSMP,TISHKOFF,YUSUKE,20.950050
MTRRchr578915057891506rs16879334+CC/Gsinglemissense111000GENOMES,AFFY,CLINSEQ_SNP,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,PERLEGEN,SEATTLESEQ,SSMP,TISHKOFF,20.956700
MTRRchr578971907897191rs10380+CC/Tsinglemissense251000GENOMES,AFFY,APPLERA_GI,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,EXOME_CHIP,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,LEE,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,PJP,SEATTLESEQ,SEQUENOM,SI_EXO,SNP500CANCER,SSMP,TISHKOFF,YUSUKE,20.811339
SDHAchr5223629223630rs1061518+TG/Tsinglemissense1LEE,20.100000
SDHAchr5223645223646rs34635677+AA/Tsinglemissense71000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,LARRIBA,NHLBI-ESP,SI_EXO,20.967633
SDHAchr5233692233693rs1062468+GA/Gsinglemissense2LEE,SEQUENOM,20.120000
SDHAchr5236618236619rs201741295+TC/Tsinglemissense1CLINSEQ_SNP,20.015500
SDHAchr5236627236628rs201139275+CC/Tsinglemissense2CLINSEQ_SNP,EXOME_CHIP,20.962500
SDHAchr5236648236649rs76896145+CC/Tsinglemissense41000GENOMES,CLINSEQ_SNP,EXOME_CHIP,GMI,20.888782
SDHAchr5236675236676rs138277996+GA/Gsinglemissense31000GENOMES,CLINSEQ_SNP,EXOME_CHIP,20.071620
SDHAchr5236677236678rs111387770+GA/Gsinglemissense51000GENOMES,BCM-HGSC-SUB,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,20.122482
SDHAchr5254511254512rs1126568+GA/Gsinglemissense31000GENOMES,LEE,SEQUENOM,20.014233
SDHAchr5254598254599rs6960+AA/Tsinglemissense9BCMHGSC_JDW,BCM_SSAHASNP,CGAP-GAI,CLINSEQ_SNP,EXOME_CHIP,LEE,NHLBI-ESP,SSMP,WI_SSAHASNP,20.864915
SDHAchr5256508256509rs6962+GA/Gsinglemissense191000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,HGSV,ILLUMINA,LARRIBA,LEE,NHLBI-ESP,PJP,SEATTLESEQ,SSMP,TISHKOFF,WI_SSAHASNP,20.177438
ENPP1chr6132129362132129363rs200362492+CA/Csinglemissense11000GENOMES,20.046832
ENPP1chr6132172367132172368rs1044498+AA/Csinglemissense321000GENOMES,ABI,AFFY,APPLERA_GI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGBASE,IBARROSO,ILLUMINA,ILLUMINA-UK,IMCJ-GDT,LEE,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,PERLEGEN,PJP,SC_SNP,SEATTLESEQ,SHGC,SSAHASNP,SSMP,TISHKOFF,20.654913
ENPP1chr6132198238132198239rs79079368+CC/Gsinglemissense71000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SSMP,TISHKOFF,20.986298
ENPP1chr6132201075132201076rs115371819+GA/Gsinglemissense61000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,TISHKOFF,20.013580
ENPP1chr6132206078132206079rs28933977+CC/Tsinglemissense91000GENOMES,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,OMIM-CURATED-RECORDS,PERLEGEN,SSMP,20.975029
ENPP3chr6132030136132030137rs200752094+TA/Tsingleintron,missense1CLINSEQ_SNP,20.011500
ENPP3chr6132030559132030560rs200750273+GA/Gsingleintron,missense3CLINSEQ_SNP,EXOME_CHIP,GMI,20.065065
ENPP3chr6132030965132030966rs202051647+GC/Gsingleintron,missense4CLINSEQ_SNP,EXOME_CHIP,GMI,SSMP,20.095500
ENPP3chr6132031140132031141rs202093315+AA/Csingleintron,missense1CLINSEQ_SNP,20.986500
ENPP3chr6132045179132045180rs58038770+AA/Gsinglemissense81000GENOMES,CLINSEQ_SNP,EXOME_CHIP,HGSV,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,SEATTLESEQ,20.987960
ENPP3chr6132047244132047245rs9321309+GA/Gsinglemissense131000GENOMES,AFFY,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PJP,SC_SNP,SSMP,TISHKOFF,WI_SSAHASNP,20.022033
ENPP3chr6132058567132058568rs77610153+CC/Gsinglemissense41000GENOMES,EXOME_CHIP,ILLUMINA,NHLBI-ESP,20.984903