Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs553668
ADRA2A
0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 8
rs7690819 1.000 0.040 4 111199502 intergenic variant A/G;T snv 3
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1364181648
SHOC1
0.925 0.080 9 111738418 missense variant A/G snv 8.0E-06 3
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2230774
ROCK2
0.807 0.240 2 11218994 missense variant G/C;T snv 0.49 12
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs3917356
IL1B
0.882 0.160 2 112834786 intron variant C/T snv 0.39 4
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs10885390 0.925 0.080 10 112881038 regulatory region variant T/A snv 0.30 3
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7100927
TCF7L2
0.925 0.080 10 113036289 intron variant A/G snv 0.54 3
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
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