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
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
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
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 13
rs2699887 0.763 0.280 3 179148620 intron variant C/T snv 0.18 11
rs772110575 0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 7
rs141178472 0.925 0.080 3 179234393 3 prime UTR variant T/C snv 3.0E-03 3.3E-03 2
rs1057519930 1.000 0.080 3 179199142 missense variant G/T snv 1