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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54