Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs10222633 0.925 0.080 3 122258079 intron variant G/A snv 0.45 4
rs10934578 0.925 0.080 3 122258435 intron variant G/T snv 0.30 4