Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs229541 0.807 0.200 22 37195278 intron variant G/A snv 0.49 2
rs229526 1.000 0.120 22 37185382 missense variant G/C;T snv 0.19; 4.0E-06 1