Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10224210 1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs760077 0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs73728279 1.000 0.080 7 151714408 intron variant G/A;T snv 4