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
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs41423247 0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs33388 0.776 0.360 5 143317730 intron variant A/T snv 0.53 12