Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918134 1.000 3 49022497 missense variant G/A;C snv 4.0E-06 1
rs121918135 1.000 3 49022903 missense variant G/C snv 1
rs138275059 1.000 3 49023111 missense variant C/G;T snv 4.0E-06; 4.0E-06 1