Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs5918 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs750257282 1.000 0.040 11 3038127 missense variant C/G;T snv 3.2E-05 3