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
rs1517352 0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs3821236 0.882 0.160 2 191038032 intron variant G/A snv 0.25 3
rs10931481 0.827 0.240 2 191090126 intron variant G/A snv 0.66 2
rs7601754 0.882 0.160 2 191075725 intron variant G/A;T snv 2
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
rs16833239 1.000 0.080 2 191075534 intron variant G/A snv 8.0E-02 1
rs7594501 1.000 0.080 2 191073874 intron variant G/A snv 8.7E-02 1