Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11676272 1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 2
rs6545814 2 24908447 intron variant A/G snv 0.53 2
rs7586879 2 24894108 intron variant C/T snv 0.47 2