Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 8
rs8126 0.807 0.080 14 103137232 3 prime UTR variant C/T snv 0.63 8
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs115797771 0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs12108497 0.851 0.080 4 184650403 intron variant C/G;T snv 6
rs1760893 0.807 0.080 14 20412501 intron variant C/A snv 0.89 6
rs1924966 0.807 0.080 13 72432915 intergenic variant T/G snv 0.33 6
rs2269772 0.925 0.080 17 50072022 synonymous variant C/T snv 0.17 0.19 6
rs3130 0.882 0.080 4 15968315 3 prime UTR variant T/A;C snv 6
rs5273 0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02 6
rs9471643
PGC
0.882 0.080 6 41751177 intron variant G/C snv 0.19 6
rs10509670 0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs10739971 0.882 0.080 9 94175398 intron variant G/A;C snv 5
rs11187842 0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 5
rs2070803 0.925 0.080 1 155185239 intron variant G/A snv 0.55 5
rs2275008 0.827 0.080 14 20448090 non coding transcript exon variant T/A;C snv 4.0E-06; 0.26 5
rs28933369 0.925 0.080 17 39724744 missense variant G/A snv 5
rs587780537 0.925 0.080 16 68810224 missense variant G/A snv 5
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs1002765 0.851 0.080 3 87227912 intron variant G/A;C snv 4
rs1051690 0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 4
rs11869286 0.925 0.080 17 39657603 intron variant G/C snv 0.52 4
rs1200055659 0.851 0.080 1 153614902 missense variant G/A snv 7.0E-06 4
rs121224 0.851 0.080 17 31574981 intron variant G/C snv 0.66 4
rs1305398818 0.925 0.080 4 88131886 missense variant G/A;C snv 4.0E-06; 4.0E-06 4