Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7200543 16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs9393903 6 11042676 intron variant G/A snv 0.18 3
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81