Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs120074172
HGD
1.000 0.080 3 120633223 missense variant T/C snv 3.6E-05; 4.0E-06 1.2E-04 1
rs120074173
HGD
1.000 0.080 3 120633233 missense variant T/C snv 1.7E-04 3.0E-04 1
rs120074174
HGD
1.000 0.080 3 120641660 missense variant C/A;T snv 5.6E-05 1
rs754428438
HGD
1.000 0.080 3 120641595 missense variant G/A;T snv 4.0E-06; 8.0E-06 1