Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 17
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs866775781 0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519985 0.724 0.360 17 7673763 missense variant T/A;C;G snv 16
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 16
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 16
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 16
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 15
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 15