Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909250 1.000 0.040 13 110719736 missense variant G/C snv 1
rs121909251 1.000 0.040 13 110719739 missense variant A/G snv 1
rs121909252 1.000 0.040 13 110719667 missense variant C/A snv 1