Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 13 | ||
rs104894833 | 0.776 | 0.280 | X | 101403984 | missense variant | C/G | snv | 1.2E-04 | 1.9E-05 | 11 | |
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs1317947 | 1.000 | 0.080 | 11 | 102617342 | intron variant | G/A | snv | 0.41 | 2 | ||
rs1423621991 | 11 | 102796745 | missense variant | C/T | snv | 1 | |||||
rs679620 | 0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 | 17 | |
rs2282377 | 1.000 | 0.080 | 14 | 104105483 | intron variant | C/G | snv | 0.12 | 0.12 | 2 | |
rs2569512 | 0.925 | 0.080 | 19 | 10679486 | intron variant | T/C | snv | 0.76 | 5 | ||
rs1556446493 | X | 108668328 | missense variant | G/T | snv | 3 | |||||
rs1933182 | 1.000 | 0.080 | 1 | 109457216 | intergenic variant | A/C | snv | 0.63 | 3 | ||
rs2208338 | 1.000 | 0.080 | 6 | 11028421 | intron variant | G/A | snv | 0.21 | 2 | ||
rs4773144 | 0.827 | 0.080 | 13 | 110308365 | intron variant | A/G | snv | 0.42 | 7 | ||
rs12194000 | 1.000 | 0.080 | 6 | 110454809 | intron variant | A/G;T | snv | 2 | |||
rs10794720 | 1.000 | 0.080 | 10 | 1110225 | intron variant | T/C | snv | 0.89 | 4 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 41 | ||
rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 22 | |
rs2230774 | 0.807 | 0.240 | 2 | 11218994 | missense variant | G/C;T | snv | 0.49 | 12 | ||
rs2074388 | 1.000 | 4 | 112431241 | missense variant | G/A | snv | 0.62 | 0.65 | 3 | ||
rs2074379 | 1.000 | 4 | 112431743 | missense variant | G/A | snv | 0.62 | 0.65 | 3 | ||
rs2074380 | 4 | 112432155 | missense variant | G/A;T | snv | 8.5E-03; 2.4E-05 | 2 | ||||
rs2074381 | 4 | 112432293 | missense variant | A/G | snv | 8.5E-03 | 5.5E-03 | 2 | |||
rs7901695 | 0.851 | 0.160 | 10 | 112994329 | intron variant | T/C | snv | 0.34 | 6 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
rs6046 | 0.925 | 0.080 | 13 | 113118845 | missense variant | G/A;C;T | snv | 0.13 | 5 | ||
rs814698 | 1.000 | 0.080 | 9 | 113967563 | intron variant | A/T | snv | 0.22 | 2 |