Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7775698 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs11066301 0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs9402686 6 135106679 upstream gene variant G/A snv 0.20 4