Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 6
rs11864909 0.851 0.160 16 20389517 intron variant C/T snv 0.23 4
rs115114609 1.000 0.080 5 88448197 intron variant G/A snv 3.4E-02 2