Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2285053 0.752 0.320 16 55478465 intron variant C/T snv 0.12 15
rs11643630 0.925 0.080 16 55476547 intron variant T/G snv 0.55 2
rs11644561 0.925 0.080 16 55475122 intron variant G/A snv 0.20 2