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
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
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24