Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs1130233 0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs12229892 0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs11536878 0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs158572 0.851 0.120 5 60943616 intron variant G/A snv 0.63 4
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs2301756 0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs3805246 0.882 0.120 4 143382955 intron variant G/A snv 0.31 3
rs6912200
PGC
0.925 0.080 6 41750170 intron variant C/T snv 0.54 3