Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10832169 11 14044939 intron variant G/A snv 0.39 1
rs11023056 11 14030572 intron variant A/G snv 0.48 1
rs2618521 11 14031785 intron variant A/G snv 0.66 1