Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs442495 1.000 0.080 15 58730416 intron variant T/C snv 0.49 1
rs4238331 15 58719934 intron variant T/G snv 0.63 1
rs12911832 1.000 0.040 15 58693705 intron variant A/T snv 0.38 1