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 8
rs10168266 0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 1
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 1
rs13426947 0.925 0.200 2 191068528 3 prime UTR variant G/A snv 0.20 1