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
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs523349 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12