Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519882 0.807 0.200 9 21974678 missense variant C/A snv 7
rs1057519928 0.807 0.200 3 179221147 missense variant A/C snv 8
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877 0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879 0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 10
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs867262025 0.790 0.360 3 179221146 missense variant G/A snv 10
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs267606870 0.763 0.280 15 90088703 missense variant G/A;C snv 11
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs80338963 0.776 0.280 18 51065548 missense variant C/A;G;T snv 11
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12