Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918459 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs397507520 0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs121918460 0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 27
rs397517148 0.776 0.200 2 39023128 missense variant C/T snv 27
rs1555429629 0.763 0.200 15 40729632 missense variant G/A snv 23
rs672601334 0.752 0.400 1 155904798 missense variant G/C snv 18
rs1555741826 0.776 0.280 19 49601646 frameshift variant TGCC/- delins 16
rs730881014 0.776 0.360 1 155904494 stop gained A/C;G;T snv 15
rs587776917 0.776 0.200 2 232485937 stop gained -/T delins 13
rs121913528 0.851 0.160 12 25227349 missense variant C/A;T snv 12