Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1805007 | 0.695 | 0.280 | 16 | 89919709 | missense variant | C/A;G;T | snv | 4.4E-02 | 25 | ||
rs1805008 | 0.732 | 0.240 | 16 | 89919736 | missense variant | C/T | snv | 4.7E-02 | 4.8E-02 | 16 | |
rs885479 | 0.732 | 0.280 | 16 | 89919746 | missense variant | G/A | snv | 0.15 | 8.3E-02 | 16 | |
rs2228479 | 0.763 | 0.280 | 16 | 89919532 | missense variant | G/A;C | snv | 7.8E-02; 4.0E-06 | 11 | ||
rs1805009 | 0.790 | 0.280 | 16 | 89920138 | missense variant | G/A;C | snv | 4.0E-06; 9.1E-03 | 9 | ||
rs1805005 | 0.827 | 0.080 | 16 | 89919436 | missense variant | G/T | snv | 8.6E-02 | 8.0E-02 | 8 | |
rs1805006 | 0.790 | 0.080 | 16 | 89919510 | missense variant | C/A;G | snv | 5.2E-03; 4.0E-06 | 8 | ||
rs1110400 | 1.000 | 0.040 | 16 | 89919722 | missense variant | T/C | snv | 5.6E-03 | 6.6E-03 | 3 | |
rs34090186 | 0.882 | 0.080 | 16 | 89919458 | missense variant | G/A | snv | 9.6E-04 | 2.7E-04 | 3 | |
rs11547464 | 1.000 | 0.040 | 16 | 89919683 | missense variant | G/A | snv | 5.3E-03 | 4.7E-03 | 2 | |
rs1232525952 | 0.925 | 0.080 | 16 | 89919597 | synonymous variant | G/A | snv | 8.1E-06 | 2 | ||
rs1340863788 | 0.925 | 0.080 | 16 | 89919595 | missense variant | C/A;T | snv | 2 | |||
rs371055548 | 0.925 | 0.080 | 16 | 89919798 | synonymous variant | C/T | snv | 2.4E-05 | 2.1E-05 | 2 | |
rs201326893 | 1.000 | 0.040 | 16 | 89919714 | stop gained | C/A | snv | 8.4E-04 | 5.4E-04 | 1 | |
rs374827260 | 1.000 | 0.040 | 16 | 89919608 | missense variant | A/G;T | snv | 4.1E-06; 1.2E-05 | 1 |