Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs13389408 0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02 4
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 3
rs11893432 0.827 0.120 2 191057148 intron variant C/G snv 0.21 3
rs10168266 0.776 0.400 2 191071078 intron variant C/T snv 0.19 2
rs6749371 0.925 0.200 2 191037458 intron variant A/T snv 7.3E-02 2
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs13426947 0.925 0.200 2 191068528 3 prime UTR variant G/A snv 0.20 1