Folate SNP Data


Gene SymbolChromosomeStartEndrs IDStrandNCBI refObservedFunctionSubmitter CountSubmitterFrequency CountAllele Frequency
TYMS chr 18658063658064rs2853533+GC/Gintron,missense151000GENOMES,BGI,BUSHMAN,CGAP-GAI,ENSEMBL,EXOME_CHIP,GMI,HGSV,ILLUMINA,MGC_GENOME_DIFF,NHLBI-ESP,SC_J20.316397
TYMS chr 18671025671026rs2853534+CC/Tintron,untransl181000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUM20.518028
TYMS chr 18671056671057rs2853535+CC/Tintron,untransl191000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUM20.517115
TYMS chr 18671519671520rs2853536+CC/Tintron,untransl181000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,P20.515632
TYMS chr 18671647671648rs2853537+AA/Tintron,untransl151000GENOMES,ABI,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,PJP,20.507916
TYMS chr 18672287672288rs2853538+CC/Tintron,untransl161000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUM20.515718
TYMS chr 18659828659829rs2853539+AA/Gintron,near-gen201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,E20.400182
TYMS chr 18657684657685rs2853542+GC/Gintron,untransl51000GENOMES,CGAP-GAI,COMPLETE_GENOMICS,SC_JCM,SSMP,20.38578
TYMS chr 18666506666507rs2853543+CC/Gintron191000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOM20.488242
TYMS chr 18671104671105rs2853740+TC/Tintron,untransl191000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUM20.435435
TYMS chr 18658169658170rs28602966+GG/Tintron,nonsense61000GENOMES,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SSAHASNP,SSMP,20.983012
TYMS chr 18662521662522rs2925470-TA/Tintron31000GENOMES,GMI,SC_JCM,20.650138
TYMS chr 18666272666273rs34007153+CA/Cintron31000GENOMES,ILLUMINA,SNP500CANCER,20.022047
TYMS chr 18673450673451rs34489327+T-/TTAintron,cds-inde1SNP500CANCER,20.470052
TYMS chr 18666264666265rs34502878+CC/Tintron51000GENOMES,BGI,GMI,SNP500CANCER,SSMP,20.933872
TYMS chr 18657645657730rs34743033+CClengtunknown1SNP500CANCER,30.336816
TYMS chr 18669295669295rs34795969+--/ATTintron1SNP500CANCER,20.520154
TYMS chr 18670471670472rs35143366+CC/Tintron,untransl21000GENOMES,SNP500CANCER,20.986825
TYMS chr 18669186669187rs35710611+CC/Tintron41000GENOMES,ILLUMINA,NHLBI-ESP,SNP500CANCER,20.988754
TYMS chr 18666532666533rs36080427+GG/Tintron21000GENOMES,SNP500CANCER,20.986841
TYMS chr 18662246662247rs3786362-AC/Tcoding-synon111000GENOMES,CLINSEQ_SNP,GMI,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PHARMGKB_AB_DME,SEATTLESEQ,SSMP,20.028828
TYMS chr 18670887670888rs3826626-TA/Gintron,untransl121000GENOMES,BGI,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,GMI,ILLUMINA,NHLBI-ESP,PERLEGEN,SSMP,TISHKOFF,20.913225
TYMS chr 18658422658423rs3891167+AA/Gintron,near-gen171000GENOMES,ABI,BL,BUSHMAN,COMPLETE_GENOMICS,DEVINE_LAB,ENSEMBL,GMI,ILLUMINA-UK,PJP,SC_JCM,SEQUENOM,20.78503
TYMS chr 18657645657701rs45445694+CClengtunknown1PHARMGKB_PAAR-SJCRH,60.428094
TYMS chr 18659176659177rs4987088+GA/Gintron,near-gen31000GENOMES,PERLEGEN,SNP500CANCER,20.011754
TYMS chr 18659148659149rs4987089+AA/Gintron,near-gen31000GENOMES,PERLEGEN,SNP500CANCER,20.98898
TYMS chr 18659235659236rs502396+CC/Tintron,near-gen181000GENOMES,ABI,BCM-HGSC-SUB,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,KRIBB_YJKIM,20.627612
TYMS chr 18671049671050rs523998-TA/Gintron,untransl51000GENOMES,ABI,BCM-HGSC-SUB,BL,SC_JCM,20.964915
TYMS chr 18666099666100rs55688320+AA/Cintron7BCMHGSC_JDW,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,SSMP,20.25
TYMS chr 18666073666074rs55742849+AA/Gintron81000GENOMES,BCMHGSC_JDW,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSMP,20.883349
TYMS chr 18665840665841rs55867764+GA/Gintron41000GENOMES,GMI,HGSV,SSMP,20.01607
TYMS chr 18666031666032rs55897736+CC/Tintron61000GENOMES,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,SSMP,20.931319
TYMS chr 18666096666097rs55906508+CC/Gintron7BCMHGSC_JDW,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,SSMP,20.25
TYMS chr 18666036666037rs56380264+AA/Gintron51000GENOMES,GMI,HGSV,HUMANGENOME_JCVI,SSMP,20.93945
TYMS chr 18665842665843rs56405278+TC/Tintron41000GENOMES,GMI,HGSV,SSMP,20.011478
TYMS chr 18671976671977rs60279109+AA/Gintron,untransl111000GENOMES,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,PJP,SSMP,TISHKOFF,20.517399
TYMS chr 18666932666933rs62090121+TA/Tintron41000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,20.099083
TYMS chr 18666938666939rs62090122+AA/Tintron51000GENOMES,BCMHGSC_JDW,ENSEMBL,GMI,SSMP,20.674312
TYMS chr 18666962666963rs62090123+AA/Tintron51000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,SSMP,20.765138
TYMS chr 18660441660442rs66567989+A-/Aintron81000GENOMES,BILGI_BIOE,DEVINE_LAB,HUMANGENOME_JCVI,LUNTER,PJP,SSMP,TISHKOFF,20.072477
TYMS chr 18673015673016rs699517+CC/Tuntranslated-3241000GENOMES,AFFY,BCMHGSC_JDW,BGI,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILL20.520312
TYMS chr 18669760669764rs72086130+CT-/CTCintron61000GENOMES,BILGI_BIOE,BUSHMAN,DEVINE_LAB,LUNTER,SSMP,20.089908
TYMS chr 18658331658332rs72634355+CC/Tintron,untransl71000GENOMES,BGI,BUSHMAN,GMI,ILLUMINA,SSMP,TISHKOFF,20.712385
TYMS chr 18668519668520rs72867160+TG/Tintron71000GENOMES,BL,BUSHMAN,GMI,ILLUMINA,SSMP,TISHKOFF,20.072936
TYMS chr 18658000658001rs73366471+GA/Gintron,nonsense71000GENOMES,COMPLETE_GENOMICS,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SEATTLESEQ,TISHKOFF,20.019266
TYMS chr 18660155660156rs73366479+AA/Gintron,near-gen31000GENOMES,COMPLETE_GENOMICS,ILLUMINA,20.983945
TYMS chr 18658416658417rs75047328+GG/Tintron,near-gen41000GENOMES,GMI,SSMP,TISHKOFF,20.989556
TYMS chr 18660366660367rs75075985+TA/Tintron41000GENOMES,BGI,GMI,SSMP,20.072237
TYMS chr 18658034658035rs77400748+AA/Gcoding-synon,in41000GENOMES,GMI,NHLBI-ESP,SSMP,20.977961
TYMS chr 18669839669840rs77404636+TC/Tintron41000GENOMES,BGI,GMI,SSMP,20.073977
TYMS chr 18667820667821rs78835614+CC/Tintron51000GENOMES,BGI,GMI,ILLUMINA,SSMP,20.926458
TYMS chr 18664751664752rs79833699+CC/Tintron41000GENOMES,ENSEMBL,GMI,SSMP,20.637156
TYMS chr 18666624666625rs8088781+CC/Tintron71000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SNP500CANCER,SSMP,TISHKOFF,WI_SSAHASNP,20.910945