Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519928 0.807 0.200 3 179221147 missense variant A/C snv 8
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 10
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
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
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
rs1057519951 0.882 0.080 3 49375472 missense variant C/G;T snv 4
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs867262025 0.790 0.360 3 179221146 missense variant G/A snv 10