Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs3764880 0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs7453920 0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs5743704 0.763 0.240 4 153704799 missense variant C/A snv 2.8E-02 2.8E-02 9
rs10766197 0.807 0.240 11 14900334 upstream gene variant G/A;C snv 6