Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519862 0.851 0.160 17 39723405 missense variant G/A snv 5
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
rs1057519962 0.827 0.160 18 51067035 missense variant G/A;T snv 6
rs121912580 0.807 0.280 18 51067036 missense variant G/A;C;T snv 7
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 9
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
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs121913407 0.763 0.240 3 41224645 missense variant T/C;G snv 10
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 10
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 11
rs1057519886 0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs1057520005 0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 11
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs730882026 0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12