Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs1057520010 0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs1057519886 0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
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
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 11
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
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 10
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs121913407 0.763 0.240 3 41224645 missense variant T/C;G snv 10
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 10
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 9