Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10419226 | 0.925 | 0.080 | 19 | 18692362 | intron variant | T/G | snv | 0.67 | 2 | ||
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
rs11789015 | 0.882 | 0.080 | 9 | 93953746 | intron variant | A/C;G | snv | 1 | |||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 10 | |
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 14 | |
rs2687201 | 0.925 | 0.080 | 3 | 70879779 | intergenic variant | A/C;G | snv | 1 | |||
rs3784262 | 0.882 | 0.160 | 15 | 57960908 | intron variant | T/A;C | snv | 1 | |||
rs6449586 | 1.000 | 0.080 | 5 | 51339044 | intergenic variant | C/T | snv | 0.64 | 1 | ||
rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 6 | |||
rs9257809 | 0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 | 4 | ||
rs9936833 | 0.882 | 0.160 | 16 | 86369512 | intergenic variant | C/T | snv | 0.64 | 3 |