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
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs2279343 0.776 0.200 19 41009358 missense variant A/G snv 0.13 8