Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7209436 0.851 0.200 17 45792776 intron variant C/T snv 0.43 5
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs7867155 0.925 0.080 9 96065532 intron variant C/T snv 0.13 2
rs8067056 0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9980603 0.925 0.080 21 40514656 intron variant T/C snv 0.40 2