Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 17
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 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
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G 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
rs1057519985 0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 14
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 14
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs377767347 0.742 0.520 18 51065549 missense variant G/A;C;T snv 13
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12