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
rs1057519956 0.827 0.200 2 218583025 missense variant T/C snv 5
rs1057519957 0.827 0.200 2 218583026 missense variant C/G snv 5
rs1057519886 0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 12
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913407 0.763 0.240 3 41224645 missense variant T/C;G snv 12
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs121913228 0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs28931588 0.701 0.200 3 41224606 missense variant G/A;C;T snv 17
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 17
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23