Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs375422359 1.000 0.040 2 178563634 missense variant C/T snv 2.4E-05 3.5E-05 1
rs764005465 1.000 0.040 2 178572808 missense variant C/T snv 8.1E-06 1