Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10849448 | 0.807 | 0.120 | 12 | 6384185 | 5 prime UTR variant | A/G | snv | 0.82 | 6 | ||
rs7127214 | 0.807 | 0.120 | 11 | 36322143 | intron variant | C/G;T | snv | 6 | |||
rs149850873 | 0.807 | 0.120 | 18 | 12885121 | intron variant | G/A | snv | 1.7E-02 | 6 | ||
rs45539732 | 0.807 | 0.120 | 2 | 191009521 | intron variant | T/C | snv | 1.9E-02 | 6 | ||
rs11714843 | 0.807 | 0.120 | 3 | 119502217 | intron variant | T/A | snv | 0.15 | 6 | ||
rs3825568 | 0.807 | 0.120 | 14 | 68793871 | 5 prime UTR variant | C/G;T | snv | 6 | |||
rs1279094 | 0.882 | 0.120 | 9 | 11706771 | intron variant | T/C | snv | 0.43 | 3 | ||
rs1823549 | 0.882 | 0.120 | 1 | 102682275 | intergenic variant | T/C | snv | 0.89 | 3 | ||
rs41291794 | 0.882 | 0.120 | 6 | 32457985 | downstream gene variant | A/T | snv | 7.5E-02 | 3 | ||
rs481331 | 0.882 | 0.120 | 10 | 42507600 | intergenic variant | A/T | snv | 0.80 | 3 | ||
rs72632736 | 0.882 | 0.120 | 1 | 4389144 | intergenic variant | A/G | snv | 4.3E-02 | 3 | ||
rs1178121 | 0.882 | 0.120 | 7 | 18723029 | intron variant | C/A | snv | 0.31 | 3 | ||
rs114940806 | 0.882 | 0.120 | 1 | 44093000 | intron variant | A/G | snv | 5.4E-02 | 3 | ||
rs12517545 | 0.882 | 0.120 | 5 | 74384489 | intron variant | G/A | snv | 0.13 | 3 | ||
rs864089 | 0.882 | 0.120 | 3 | 64258442 | intron variant | T/C | snv | 0.22 | 3 | ||
rs79575701 | 0.882 | 0.120 | 18 | 48053250 | intron variant | C/A;T | snv | 3 |