Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs1494555 0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs735665 0.776 0.280 11 123490689 intron variant G/A snv 0.15 8