Riboflavin SNP Data


Gene SymbolChromosomeStartEndrs IDStrandNCBI refObservedClassFunctionSubmitter CountSubmitterFrequency CountAllele Frequency
ACAD9chr3128607293128607294rs114417154+CC/Tsingleintron21000GENOMES,TISHKOFF,20.979530
ACAD9chr3128607378128607379rs115046806+GA/Gsingleintron11000GENOMES,20.033072
ACAD9chr3128607383128607384rs62268187+TG/Tsingleintron41000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,20.044495
ACAD9chr3128607467128607468rs73208002+CA/Csingleintron11000GENOMES,20.032637
ACAD9chr3128607521128607521rs201108858+--/Ainsertionintron31000GENOMES,LUNTER,SSMP,20.961433
ACAD9chr3128607646128607647rs150895592+T-/Tdeletionintron21000GENOMES,LUNTER,20.012397
ACAD9chr3128608195128608196rs6786847+CC/Tsingleintron51000GENOMES,BCM_SSAHASNP,COMPLETE_GENOMICS,ILLUMINA-UK,TISHKOFF,20.934005
ACAD9chr3128608299128608300rs62268188+GA/Gsingleintron51000GENOMES,BCMHGSC_JDW,ENSEMBL,SSMP,TISHKOFF,20.054587
ACAD9chr3128608340128608341rs2929859+TG/Tsingleintron151000GENOMES,ABI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PJP,SC_JCM,SSMP,TISHKOFF,20.341241
ACAD9chr3128608578128608579rs13073796+TG/Tsingleintron111000GENOMES,ABI,BCM-HGSC-SUB,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.108424
ACAD9chr3128608750128608751rs6790091+GC/Gsingleintron151000GENOMES,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_SNP,SSMP,TISHKOFF,WUGSC_SSAHASNP,20.456700
ACAD9chr3128608977128608977rs199961338+--/Tinsertionintron31000GENOMES,SSMP,TISHKOFF,20.983471
ACAD9chr3128609025128609026rs150454584+GA/Gsingleintron11000GENOMES,20.031221
ACAD9chr3128609197128609198rs13434000+GA/Gsingleintron61000GENOMES,COMPLETE_GENOMICS,HGSV,ILLUMINA-UK,TISHKOFF,WUGSC_SSAHASNP,20.082342
ACAD9chr3128609254128609255rs13434201+TA/Tsingleintron61000GENOMES,BUSHMAN,ILLUMINA-UK,SSMP,TISHKOFF,WUGSC_SSAHASNP,20.118132
ACAD9chr3128609283128609284rs142912887+GA/Gsingleintron11000GENOMES,20.031221
ACAD9chr3128609310128609311rs71331617+CC/Tsingleintron81000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,HUMANGENOME_JCVI,SSMP,TISHKOFF,20.555199
ACAD9chr3128609326128609327rs148035542+TC/Tsingleintron31000GENOMES,SSMP,TISHKOFF,20.055096
ACAD9chr3128609522128609523rs141759595+CC/Tsingleintron21000GENOMES,SSMP,20.962810
ACAD9chr3128609678128609679rs114145289+TC/Tsingleintron31000GENOMES,ILLUMINA,TISHKOFF,20.022213
ACAD9chr3128609701128609702rs184937941+TG/Tsingleintron11000GENOMES,20.015611
ACAD9chr3128609745128609746rs139643158+GA/Gsingleintron11000GENOMES,20.011938
ACAD9chr3128609976128609977rs78314245+CC/Tsingleintron41000GENOMES,ILLUMINA-UK,SSMP,TISHKOFF,20.982569
ACAD9chr3128610014128610015rs62268189+AA/Gsingleintron51000GENOMES,BCMHGSC_JDW,ENSEMBL,SSMP,TISHKOFF,20.945413
ACAD9chr3128610628128610629rs6791451+TC/Tsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,20.641900
ACAD9chr3128612085128612088rs145182927+ATG-/ATGdeletionintron21000GENOMES,LUNTER,20.032599
ACAD9chr3128612112128612113rs1683811+AA/Csingleintron111000GENOMES,ABI,BL,BUSHMAN,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,20.664227
ACAD9chr3128612228128612229rs6806468+AA/Tsingleintron91000GENOMES,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,HGSV,ILLUMINA-UK,PJP,TISHKOFF,WI_SSAHASNP,20.909906
ACAD9chr3128612561128612562rs10460833+AA/Gsingleintron101000GENOMES,BCMHGSC_JDW,BUSHMAN,ENSEMBL,ILLUMINA,PERLEGEN,PJP,SC_SNP,SSMP,TISHKOFF,20.943250
ACAD9chr3128612658128612659rs1680780+GC/Gsingleintron151000GENOMES,ABI,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,20.487893
ACAD9chr3128612829128612830rs1680781+CA/Csingleintron171000GENOMES,ABI,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SSMP,TISHKOFF,20.475880
ACAD9chr3128612999128613000rs142860593+TC/Tsingleintron11000GENOMES,20.016070
ACAD9chr3128613142128613143rs62268190+AA/Gsingleintron61000GENOMES,BCMHGSC_JDW,ENSEMBL,PJP,SSMP,TISHKOFF,20.944037
ACAD9chr3128613390128613391rs57147056+TA/Tsingleintron61000GENOMES,ENSEMBL,HGSV,HUMANGENOME_JCVI,PJP,SSMP,20.111366
ACAD9chr3128613523128613524rs79986808+GA/Gsingleintron41000GENOMES,GMI,SSMP,TISHKOFF,20.077894
ACAD9chr3128613526128613527rs150053865+CC/Tsingleintron11000GENOMES,20.987603
ACAD9chr3128613765128613766rs140879975+CC/Gsingleintron31000GENOMES,SSMP,TISHKOFF,20.943526
ACAD9chr3128613843128613844rs144311840+TC/Tsingleintron31000GENOMES,SSMP,TISHKOFF,20.054178
ACAD9chr3128614003128614004rs143463639+GA/Gsingleintron11000GENOMES,20.031221
ACAD9chr3128614132128614133rs1683791+CC/Tsingleintron221000GENOMES,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.355979
ACAD9chr3128614184128614185rs1680778+AA/Csinglecoding-synon,ncRNA241000GENOMES,ABI,AFFY,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,MGC_GENOME_DIFF,NHLBI-ESP,PERLEGEN,PJP,SC_JCM,SEATTLESEQ,SSMP,TISHKOFF,30.501608
ACAD9chr3128614539128614540rs62268191+CC/Tsingleintron61000GENOMES,BCMHGSC_JDW,BUSHMAN,ENSEMBL,SSMP,TISHKOFF,20.945005
ACAD9chr3128614562128614562rs111842935+--/CTC/TCinsertionintron,cds-indel21000GENOMES,BUSHMAN,30.365138
ACAD9chr3128614565128614565rs200704935+--/Cinsertionintron11000GENOMES,20.420569
ACAD9chr3128614769128614770rs1680779+GA/Gsingleintron161000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,20.535933
ACAD9chr3128616301128616304rs201894239+GAG-/GAGdeletionintron21000GENOMES,LUNTER,20.011938
ACAD9chr3128616324128616325rs1683804+CC/Tsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.346939
ACAD9chr3128616358128616359rs789213-CC/Gsingleintron161000GENOMES,ABI,AFFY,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,KRIBB_YJKIM,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.341772
ACAD9chr3128616715128616716rs76764354+TA/Tsingleintron11000GENOMES,20.013490
ACAD9chr3128616751128616752rs34638819+GA/Gsingleintron101000GENOMES,ABI,BCM-HGSC-SUB,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,20.112077
ACAD9chr3128617248128617249rs79398737+TG/Tsingleintron21000GENOMES,ILLUMINA-UK,20.035780
ACAD9chr3128617331128617331rs200124262+-lengthTooLongin-delintron21000GENOMES,TISHKOFF,20.966942
ACAD9chr3128617412128617412rs147931805+--/Tinsertionintron21000GENOMES,LUNTER,20.951791
ACAD9chr3128617425128617426rs73210606+AA/Gsingleintron11000GENOMES,20.966493
ACAD9chr3128617789128617790rs1979528+TG/Tsingleintron71000GENOMES,ABI,BCMHGSC_JDW,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.071192
ACAD9chr3128618282128618283rs1979529+TC/Tsinglecoding-synon,ncRNA101000GENOMES,BCMHGSC_JDW,CLINSEQ_SNP,CORNELL,CSHL-HAPMAP,ENSEMBL,ILLUMINA,NHLBI-ESP,SSMP,TSC-CSHL,20.028382
ACAD9chr3128618365128618366rs2340466+GC/G/Tsingleintron31000GENOMES,SC_JCM,TSC-CSHL,30.003484
ACAD9chr3128618770128618771rs73210607+AA/Gsingleintron11000GENOMES,20.967363
ACAD9chr3128619165128619166rs149575458+CC/Tsingleintron11000GENOMES,20.968779
ACAD9chr3128619236128619237rs115225846+CC/Tsingleintron11000GENOMES,20.966928
ACAD9chr3128619323128619324rs62268192+GA/Gsingleintron41000GENOMES,BCMHGSC_JDW,ENSEMBL,SSMP,20.054587
ACAD9chr3128619356128619357rs813732-CA/Gsingleintron161000GENOMES,ABI,BCM_SSAHASNP,BGI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KWOK,PJP,SSAHASNP,SSMP,TISHKOFF,20.458410
ACAD9chr3128619357128619358rs148551394+GA/Gsingleintron21000GENOMES,SSMP,20.054178
ACAD9chr3128619483128619484rs142564404+GG/Tsingleintron11000GENOMES,20.983930
ACAD9chr3128619504128619505rs16852133+TC/Tsingleintron31000GENOMES,PERLEGEN,SSMP,20.054741
ACAD9chr3128619682128619683rs6809299+GA/Gsingleintron121000GENOMES,ABI,BCM-HGSC-SUB,BCM_SSAHASNP,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.121683
ACAD9chr3128619734128619735rs6809152+CC/Tsingleintron111000GENOMES,ABI,BCM-HGSC-SUB,BCM_SSAHASNP,COMPLETE_GENOMICS,ENSEMBL,GMI,PJP,SSAHASNP,SSMP,TISHKOFF,20.878552
ACAD9chr3128620003128620004rs76439060+CC/Tsingleintron31000GENOMES,GMI,SSMP,20.988686
ACAD9chr3128620267128620268rs146195726+C-/Cdeletionintron31000GENOMES,SSMP,WARNICH_LAB,20.037190
ACAD9chr3128620387128620388rs1680795-TA/Gsingleintron111000GENOMES,ABI,BCM_SSAHASNP,BL,BUSHMAN,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,SC_JCM,SSMP,20.706581
ACAD9chr3128620389128620390rs1680794-AC/Tsingleintron161000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,20.517966
ACAD9chr3128620405128620406rs115920138+CC/Tsingleintron11000GENOMES,20.980836
ACAD9chr3128620725128620726rs73862591+GG/Tsingleintron31000GENOMES,ILLUMINA-UK,TISHKOFF,20.983486
ACAD9chr3128620754128620755rs115385161+TC/Tsingleintron11000GENOMES,20.018293
ACAD9chr3128621039128621040rs7639482+CC/Tsingleintron51000GENOMES,BCMHGSC_JDW,ENSEMBL,SSMP,WI_SSAHASNP,20.946379
ACAD9chr3128621362128621363rs7617561+AA/Gsingleintron101000GENOMES,BCMHGSC_JDW,BUSHMAN,CLINSEQ_SNP,ENSEMBL,ILLUMINA,NHLBI-ESP,PJP,SSMP,WI_SSAHASNP,20.966848
ACAD9chr3128621737128621738rs62268194+TC/Tsingleintron51000GENOMES,BCMHGSC_JDW,BUSHMAN,ENSEMBL,SSMP,20.054079
ACAD9chr3128622277128622278rs62268195+TC/Tsingleintron41000GENOMES,BCMHGSC_JDW,ENSEMBL,SSMP,20.053670
ACAD9chr3128622358128622359rs12485571+CC/Tsingleintron81000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BL,CSHL-HAPMAP,ENSEMBL,ILLUMINA,TISHKOFF,20.920018
ACAD9chr3128622604128622605rs66903181+GA/Gsingleintron71000GENOMES,BCM-HGSC-SUB,COMPLETE_GENOMICS,ENSEMBL,HUMANGENOME_JCVI,SSMP,TISHKOFF,20.121795
ACAD9chr3128622741128622742rs66521976+GA/Gsingleintron81000GENOMES,BCM-HGSC-SUB,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,SSMP,TISHKOFF,20.121795
ACAD9chr3128622759128622760rs1683776+GG/Tsingleintron141000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.695312
ACAD9chr3128622921128622922rs115532916+GA/C/GsinglencRNA,missense61000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,OMIM-CURATED-RECORDS,20.013100
ACAD9chr3128623404128623405rs73210609+CC/Tsingleintron31000GENOMES,CLINSEQ_SNP,ILLUMINA,20.974492
ACAD9chr3128623756128623757rs62265261+GG/Tsingleintron41000GENOMES,BCMHGSC_JDW,ENSEMBL,SSMP,20.962385
ACAD9chr3128623784128623785rs61096019+CC/Tsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,HGSV,SSMP,TISHKOFF,20.870302
ACAD9chr3128623965128623966rs62265262+AA/Gsingleintron41000GENOMES,BCMHGSC_JDW,ENSEMBL,SSMP,20.945872
ACAD9chr3128624006128624008rs200697619+AC-/ACdeletionintron11000GENOMES,20.057851
ACAD9chr3128624007128624008rs142176941+C-/Cdeletionintron41000GENOMES,GMI,LUNTER,SSMP,20.059688
ACAD9chr3128624302128624303rs56396516+GA/Gsingleintron31000GENOMES,HGSV,ILLUMINA,20.017406
ACAD9chr3128624503128624504rs73210611+GA/Gsingleintron11000GENOMES,20.032637
ACAD9chr3128624548128624549rs112685626+GA/Gsingleintron41000GENOMES,BCM-HGSC-SUB,ILLUMINA,SSMP,20.024369
ACAD9chr3128624771128624772rs2630252+TC/Tsingleintron141000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_JCM,SSMP,TISHKOFF,WI_SSAHASNP,20.319296
ACAD9chr3128624809128624810rs7651896+CC/Tsingleintron71000GENOMES,BCMHGSC_JDW,BUSHMAN,ENSEMBL,ILLUMINA,SSMP,WI_SSAHASNP,20.949693
ACAD9chr3128624879128624880rs1683777+TG/Tsingleintron221000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.524689
ACAD9chr3128625198128625199rs7652449+GA/Gsingleintron61000GENOMES,BCMHGSC_JDW,BUSHMAN,ENSEMBL,SSMP,WI_SSAHASNP,20.054029
ACAD9chr3128625241128625242rs35020699+CC/Tsingleintron91000GENOMES,ABI,BCM-HGSC-SUB,COMPLETE_GENOMICS,ENSEMBL,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,20.907594
ACAD9chr3128625244128625245rs7652295+CC/Tsingleintron61000GENOMES,BCMHGSC_JDW,BUSHMAN,ENSEMBL,SSMP,WI_SSAHASNP,20.945513
ACAD9chr3128625317128625318rs1680788+CC/Tsingleintron181000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,WI_SSAHASNP,20.481979
ACAD9chr3128625492128625493rs62265263+CC/Tsingleintron51000GENOMES,BCMHGSC_JDW,BUSHMAN,ENSEMBL,SSMP,20.945896