Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs686 0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs265981 0.925 0.080 5 175443899 5 prime UTR variant A/G;T snv 3