Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1172398253 0.925 0.080 1 85582045 missense variant C/T snv 4.0E-06 4
rs11801299 0.807 0.200 1 204559956 downstream gene variant G/A snv 0.16 9
rs1194338 0.925 0.080 11 65493967 upstream gene variant C/A;T snv 3
rs1194624468 1.000 0.040 8 140700895 missense variant A/T snv 1.6E-05 2
rs1196644309 1.000 0.080 1 145995155 missense variant G/A snv 3
rs1200003171 0.882 0.120 14 104775122 missense variant C/A;T snv 8.0E-06 4
rs1213469537 0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 25
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs121913430 1.000 0.080 7 55174740 missense variant G/A snv 3
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121917887 0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs121918461 0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs1223118092 2 46576601 missense variant A/G snv 1
rs1231584616 16 55485367 missense variant G/A snv 4.0E-06 1
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs12918952 0.851 0.120 16 78386878 missense variant G/A;C;T snv 7
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1329032366 0.882 0.080 4 94654530 missense variant A/G snv 4.0E-06 5
rs1332018 0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6