Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12500118 1.000 0.080 4 154423482 intron variant C/T snv 0.28 1
rs1466662 1.000 0.080 4 154426241 intron variant A/T snv 0.28 1
rs4696572 1.000 0.080 4 154433764 intron variant T/C;G snv 0.29 1