Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs736707 0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs2292305 0.882 0.080 15 39588621 missense variant A/C;G snv 4.0E-06; 0.16 4
rs850807 0.882 0.040 15 23652982 intergenic variant T/A;C snv 3
rs748128078 0.925 0.040 12 13562968 missense variant G/A snv 1.6E-05 5.6E-05 2
rs756790727 0.925 0.040 12 13562883 missense variant G/A snv 1.2E-05 2
rs879254129 0.925 0.040 12 13562977 missense variant A/G snv 4.0E-06 2