Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1036199 | 0.925 | 0.160 | 5 | 157104725 | missense variant | C/A | snv | 0.87 | 0.83 | 3 | |
rs10892279 | 1.000 | 0.120 | 11 | 118741072 | intron variant | G/A;T | snv | 0.25 | 3 | ||
rs1126407 | 0.925 | 0.200 | 1 | 236537507 | missense variant | T/A | snv | 0.61 | 0.61 | 3 | |
rs13031237 | 1.000 | 0.120 | 2 | 60908994 | intron variant | G/T | snv | 0.25 | 3 | ||
rs147846074 | 0.925 | 0.200 | 21 | 44289743 | missense variant | C/G;T | snv | 1.2E-05; 3.2E-05; 4.0E-06 | 3 | ||
rs150240657 | 0.925 | 0.120 | 11 | 47682026 | missense variant | G/A | snv | 8.7E-05 | 3.6E-04 | 3 | |
rs1953126 | 1.000 | 0.120 | 9 | 120878222 | intron variant | T/C | snv | 0.68 | 3 | ||
rs34933034 | 0.925 | 0.120 | 15 | 74787133 | intron variant | G/A;T | snv | 3 | |||
rs7573065 | 1.000 | 0.120 | 2 | 218381984 | upstream gene variant | C/A;T | snv | 3 | |||
rs11586238 | 0.925 | 0.160 | 1 | 116720516 | regulatory region variant | C/G | snv | 0.19 | 4 | ||
rs11676922 | 0.925 | 0.160 | 2 | 100190478 | intron variant | T/A | snv | 0.51 | 4 | ||
rs1310182 | 0.882 | 0.360 | 1 | 113830881 | intron variant | A/C;G | snv | 0.56 | 4 | ||
rs13315591 | 0.925 | 0.160 | 3 | 58571114 | intron variant | T/C | snv | 0.15 | 4 | ||
rs13447 | 0.882 | 0.200 | 7 | 75166663 | non coding transcript exon variant | T/A;C | snv | 1.9E-02 | 4 | ||
rs201802880 | 0.882 | 0.200 | 7 | 74779296 | missense variant | G/A | snv | 1.1E-03 | 4 | ||
rs212389 | 0.925 | 0.160 | 6 | 159068759 | non coding transcript exon variant | G/A | snv | 0.60 | 4 | ||
rs26232 | 0.925 | 0.160 | 5 | 103261019 | intron variant | C/T | snv | 0.30 | 4 | ||
rs3890745 | 0.925 | 0.200 | 1 | 2622185 | intron variant | T/C | snv | 0.40 | 4 | ||
rs6859219 | 0.925 | 0.160 | 5 | 56142753 | intron variant | C/A | snv | 0.20 | 4 | ||
rs864537 | 0.925 | 0.200 | 1 | 167442147 | intron variant | A/G | snv | 0.29 | 4 | ||
rs874040 | 0.925 | 0.160 | 4 | 26106575 | downstream gene variant | G/C | snv | 0.29 | 4 | ||
rs906868 | 0.925 | 0.120 | 2 | 30225478 | intergenic variant | G/T | snv | 0.53 | 4 | ||
rs934734 | 0.925 | 0.160 | 2 | 65368452 | intron variant | G/A;T | snv | 0.54 | 4 | ||
rs945635 | 0.882 | 0.200 | 1 | 157700500 | 5 prime UTR variant | C/A;G | snv | 5.6E-05; 0.45 | 4 | ||
rs1800520 | 0.851 | 0.200 | 21 | 44290023 | missense variant | C/A;G;T | snv | 0.14; 8.3E-06 | 5 |