Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012657750 1 151368294 missense variant G/C snv 2
rs1249051329 1 151369834 synonymous variant T/C snv 3.5E-05 2
rs771038258 1 151365837 missense variant A/G snv 8.0E-06 2.1E-05 2
rs1308703978 1 151365194 missense variant C/A;T snv 4.0E-06 1