Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29