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Gene 1 Gene 2 SNP_Id Allele Chromosome Chromosome Position Functional Class P-Value Odds Ratio PMID
ABCC8rs1799854T>T1117448704intron-variant----16873704
AKR1B1--C-106T7----0.0314.714582038
ALOX5APrs38032788733T->C1330744264intron-variant0.00360.7319288030
ANK1rs515071C>T841519462intron-variant upstream-variant-2KB1.37E-081.1822456796
AP3S2rs2028299C1590374257nc-transcript-variant utr-variant-3-prime--23029454
BTN2A1rs6929846C>T626458265utr-variant-5-prime0.00061.2521672009
C2CD4AC2CD4Brs7172432A1562104190 --0.0000011.1123945395
CCR5--52029A>G3----0.032.4116442182
CDKAL1rs7756992G620679709intron-variant----19033397
CDKAL1rs7754840C620661250intron-variant----19033397
CDKAL1rs4712523G620657333intron7.00E-201.2719401414
CDKAL1rs4712524G620657634intron3.00E-101.2218711366
CDKN2ACDKN2Brs2383208A9221320772.00E-291.3419401414
CDKN2ACDKN2Brs10811661T922134094------19033397
CLOCKrs1801260C1.526374515
CRTC2rs267598056909C>T1----0.0163.0117950019
CTBP1-AS2rs7656416C>T41260747intron-variant1.37E-081.1522456796
DUSP9rs5945329T/G23152910573intron-variant2.21E-081.3923029454
DUSP9rs5945326A23153634467intron-variant2.00E-1223945395
EPHX2--G860A8--------15845398
FABP2rs1799883Ala54Thr4119320747missense,reference0.04821.2319288030
FADS1rs174550--1161571478intron-variant0.00711.1222992776
FTOrs155890227820839
GPSM1rs11787792A9136357696Intron-variant,missense,reference1.74E-101.1523945395
GYS1rs5447M416V19--------9267990
HHEXrs7923837G1094481917------19033397
HHEXrs1111875C10927031250.000000021.1423945395
HHEXrs1111875C10927031257.00E-121.2119401414
HNF1Brs4430796G1737738049intron-variant0.0000041.1123945395
HNF2Brs1016991T>T1736058153intron-variant----16873704
HNF2Brs2668A>A1116996466intron-variant----16873704
HNF4Ars745975T>T2043034693intron-variant----16873704
IGF127060213
IGF2BP2rs1470579C3185529080intron-variant----19033397
IGF2BP2rs6769511C3185812502intron0.0000000011.2318711366
IGF2BP2rs4402960T3185511687intron-variant----19033397
IGF2BP2rs4402960T3185793899intron0.0000011.1419401414
INS27316668
IRAK1rs1059703Ser532LeuX154013378Intron-variant,missense,reference0.00660.7319288030
IRS1rs2943641C2227093745--0.00341.1522046406
JAZF1rs864745T>C728180556intron-variant0.00981.14819455301
KCNJ11rs5219T1117409572Intron-variant,missense,reference----19033397
KCNQ1rs2237892C112818521Intron-variant,nc-transcript-variant\4.00E-291.323945395
KCNQ1rs231362C112691471Intron-variant,nc-transcript-variant0.0091.1222046406
KCNQ1rs2237892C112818521intron1.00E-261.3319401414
KCNQ1rs2237897C112837316intron1.00E-161.3318711366
KLF14rs972283G7130466854--0.0171.0722046406
LEPrs791595A7128222749Intron-variant,missense,reference2.55E-131.1723945395
LMNArs46411908C/T1156137743intron-variant0.06117.0316117820
MAEArs6815464G41316113intron-variant0.00000021.1223945395
MAEArs7656416 --41260747intron-variant0.000000011.1522456796
MPHOSPH9rs42756590.0121.12727115357
MTNR1Brs10930963G2182135924--0.0331.0622046406
NKX2-2rs3746741A/C2021491398downstream-variant-500B----16873704
NKX6-1rs1017560A/C485434987------16873704
PALM2rs1327796 --9109764009intron-variant0.0000031.1322456796
PAX4--Arg121Trp7--------16423628
PEPDrs3786897A1933402102intron-variant0.04071.0924086726
PRKAA2rs2051040GG157142755intron-variant0.002--16567511
PRKCB---105C>T16----0.015--16567829
PROX1rs340874--1214159256--0.00781.1222992776
PSMD6rs831571C364062621 --0.01351.1124086726
PTEN--C>G10------14623110
SLC16A13rs312457G177037074Intron-variant,missense,reference7.69E-131.223945395
SLC30A8rs13266634C8118184783missense,reference----19033397
SLC30A8rs13266634C8117172544missense2.00E-141.2219401414
SOCS2rs12425869A/G1293961353intron-variant----16406727
STK11rs741765--191221545intron-variant0.0171.3317950019
SYKrs10993738 --990870958intron-variant0.0000051.1622456796
TCF7L2rs12255372T10114808902intron-variant--1.71419033397
TCF7L2rs7903146T10112998590intron-variant2.00E-151.4823945395
TCF7L2rs7903146T10112998590intron8.00E-121.5419401414
UBE2E2rs6780569G323156993 --0.00000041.1723945395
UCP1rs10011540-112A>C4141493961------16338218
UTS2--S89N1----0.0018--15476949
ZPR1rs964184C27411854