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
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs1131691021 0.716 0.120 17 7675097 missense variant A/C;G snv 21