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
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs27072 0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs12364283 0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 3