Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs11196170
TCF7L2
0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 9
rs17747324
TCF7L2
0.925 0.160 10 112992744 intron variant T/C snv 0.17 3
rs12243326
TCF7L2
0.925 0.160 10 113029056 intron variant T/C snv 0.27 3
rs290475
TCF7L2
1.000 0.040 10 113114260 intron variant C/A;T snv 2
rs12772424
TCF7L2
1.000 0.040 10 113120792 intron variant A/T snv 0.57 2
rs4918796
TCF7L2
1.000 0.080 10 113120583 intron variant T/C snv 0.18 2
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 2
rs34872471
TCF7L2
1.000 0.080 10 112994312 intron variant T/C snv 0.29 2
rs35198068
TCF7L2
10 112995025 intron variant T/C snv 0.29 2
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 2
rs11196169
TCF7L2
10 112961478 intron variant A/G;T snv 1
rs12775879
TCF7L2
10 113144442 intron variant T/G snv 7.6E-02 1
rs386418874
TCF7L2
1.000 0.080 10 112988102 intron variant GT/-;GTGT;GTGTGT delins 1
rs117229942
TCF7L2
1.000 0.080 10 112978018 intron variant C/T snv 5.8E-03 1
rs56299331
TCF7L2
1.000 0.040 10 113028677 intron variant C/T snv 0.15 1
rs11594566
TCF7L2
10 113153211 intron variant C/T snv 0.14 1
rs4367880
TCF7L2
10 113035497 intron variant G/C;T snv 1
rs6585201
TCF7L2
10 113009024 intron variant G/A snv 0.52 1
rs880082
TCF7L2
10 113129502 5 prime UTR variant T/A snv 0.16 1
rs2104598
TCF7L2
10 112955839 intron variant G/A snv 0.55 1
rs7094871
TCF7L2
1.000 0.080 10 112952395 intron variant C/G;T snv 1
rs6585202
TCF7L2
1.000 0.080 10 113023044 intron variant T/C snv 0.53 1