Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12