Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs371769427 0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 24
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
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs753660142 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs28931588 0.701 0.200 3 41224606 missense variant G/A;C;T snv 17
rs866775781 0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs149680468 0.742 0.320 4 152326137 missense variant G/A;C;T snv 15