Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12734001 1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05 2
rs3817222 1.000 0.080 1 202495632 missense variant C/T snv 3.6E-05 7.0E-06 1