Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs6259 0.658 0.400 17 7633209 missense variant G/A snv 8.9E-02 8.1E-02 27
rs1870050 0.827 0.160 15 51344354 intron variant A/C snv 6.0E-02 5