Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs290481
TCF7L2
0.827 0.200 10 113164066 intron variant C/T snv 0.20 9
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55 9
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs12243326
TCF7L2
0.925 0.160 10 113029056 intron variant T/C snv 0.27 5
rs17747324
TCF7L2
0.925 0.160 10 112992744 intron variant T/C snv 0.17 4
rs7895340
TCF7L2
0.851 0.160 10 113041766 intron variant G/A snv 0.53 4
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 3
rs1225404
TCF7L2
0.882 0.160 10 113154906 intron variant C/T snv 0.71 3
rs34872471
TCF7L2
1.000 0.080 10 112994312 intron variant T/C snv 0.29 3
rs7100927
TCF7L2
0.925 0.080 10 113036289 intron variant A/G snv 0.54 3
rs7900150
TCF7L2
0.882 0.160 10 113034064 intron variant T/A;C snv 0.54 3
rs10885406
TCF7L2
0.925 0.120 10 113017965 intron variant A/G snv 0.55 2
rs11196175
TCF7L2
0.925 0.160 10 112976855 intron variant T/C snv 0.20 2
rs11196218
TCF7L2
0.925 0.160 10 113080735 intron variant G/A snv 0.25 2
rs11196229
TCF7L2
0.925 0.160 10 113106413 intron variant G/A snv 0.19 2
rs11196236
TCF7L2
0.925 0.160 10 113127963 intron variant T/C snv 0.16 2
rs1427214163
TCF7L2
1.000 0.080 10 113151879 missense variant C/T snv 7.0E-06 2
rs3814573
TCF7L2
1.000 0.080 10 113138334 intron variant T/C snv 0.71 2
rs4132670
TCF7L2
1.000 0.080 10 113008012 intron variant G/A snv 0.39 2
rs4918796
TCF7L2
1.000 0.080 10 113120583 intron variant T/C snv 0.18 2