Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 1
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs5744256
IL18
0.827 0.120 11 112152125 intron variant A/G snv 0.16 1
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 1
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55 2
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs1846594 0.925 0.120 3 113197356 intergenic variant G/A;T snv 1
rs2075533
DELEC1 ; TNFSF8
0.851 0.160 9 114931351 intron variant G/A;T snv 1
rs1600249
BLK
0.827 0.280 8 11502129 intron variant G/T snv 0.23 1
rs9387478
DCBLD1
0.851 0.080 6 117465017 intron variant C/A;T snv 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs1169300
HNF1A
0.882 0.080 12 120993422 intron variant G/A snv 0.27 1
rs2464196
HNF1A
0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 2
rs1899951
PPARG
0.851 0.160 3 12353341 intron variant C/T snv 0.26 1
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 2
rs34330
CDKN1B ; GPR19
0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 1
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 3
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 2
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4