Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1058046 | 0.925 | 0.120 | 17 | 43953163 | missense variant | G/C | snv | 0.63 | 0.59 | 2 | |
rs10885406 | 0.925 | 0.120 | 10 | 113017965 | intron variant | A/G | snv | 0.55 | 2 | ||
rs11076023 | 0.925 | 0.120 | 16 | 54118136 | 3 prime UTR variant | A/T | snv | 0.49 | 2 | ||
rs11960429 | 0.925 | 0.120 | 5 | 180739677 | missense variant | G/A | snv | 1.2E-02 | 1.5E-02 | 2 | |
rs12156368 | 0.925 | 0.120 | 8 | 18885203 | intron variant | C/T | snv | 0.36 | 2 | ||
rs1541276 | 0.925 | 0.120 | 18 | 13825728 | splice region variant | A/C | snv | 0.17 | 0.19 | 2 | |
rs1550805 | 0.925 | 0.120 | 5 | 68287979 | intron variant | C/T | snv | 6.9E-02 | 2 | ||
rs16861194 | 0.925 | 0.120 | 3 | 186841636 | upstream gene variant | A/G | snv | 0.15 | 2 | ||
rs1797 | 0.925 | 0.120 | 10 | 117945927 | intergenic variant | C/T | snv | 0.45 | 2 | ||
rs1926065 | 0.925 | 0.120 | 20 | 56256281 | intergenic variant | G/A | snv | 0.31 | 2 | ||
rs1968482 | 0.925 | 0.120 | 2 | 24863989 | intron variant | T/C | snv | 0.32 | 2 | ||
rs200027152 | 0.925 | 0.120 | 11 | 73975612 | missense variant | C/T | snv | 8.0E-05 | 4.9E-05 | 2 | |
rs201777403 | 0.925 | 0.120 | 5 | 148827105 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs2028299 | 0.925 | 0.120 | 15 | 89831025 | 3 prime UTR variant | C/A | snv | 0.72 | 2 | ||
rs2118404 | 0.925 | 0.120 | 2 | 25154460 | 3 prime UTR variant | C/A;G;T | snv | 2 | |||
rs225011 | 0.925 | 0.120 | 14 | 80205865 | intron variant | T/A;C | snv | 2 | |||
rs2302870 | 0.925 | 0.120 | 2 | 207088682 | intron variant | T/C;G | snv | 2 | |||
rs3746876 | 0.925 | 0.120 | 21 | 38299525 | synonymous variant | C/T | snv | 2.0E-02 | 3.2E-02 | 2 | |
rs4325426 | 0.925 | 0.120 | 13 | 40642300 | intron variant | C/A | snv | 0.41 | 2 | ||
rs4450508 | 0.925 | 0.120 | 18 | 60246201 | intergenic variant | G/A | snv | 0.31 | 2 | ||
rs6064099 | 0.925 | 0.120 | 20 | 54643425 | intron variant | G/C | snv | 0.30 | 0.36 | 2 | |
rs6983992 | 0.925 | 0.120 | 8 | 18871125 | intron variant | T/C | snv | 0.20 | 2 | ||
rs706713 | 0.925 | 0.120 | 5 | 68226894 | synonymous variant | C/T | snv | 0.31 | 0.31 | 2 | |
rs708277 | 0.925 | 0.120 | 16 | 54114023 | 3 prime UTR variant | G/A | snv | 0.62 | 2 | ||
rs7181866 | 0.925 | 0.120 | 15 | 50318595 | intron variant | A/G | snv | 6.6E-02 | 2 |