Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs1800498 0.882 0.080 11 113420866 intron variant G/A snv 0.44 4
rs279826 1.000 0.080 4 46332192 intron variant A/G snv 0.46 4