Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs320 | 0.827 | 0.200 | 8 | 19961566 | intron variant | T/A;G | snv | 3 | |||
rs325 | 8 | 19961817 | intron variant | T/C | snv | 9.0E-02 | 4 | ||||
rs326 | 8 | 19961928 | intron variant | A/G | snv | 0.37 | 3 | ||||
rs327 | 8 | 19962025 | intron variant | T/G | snv | 0.31 | 4 | ||||
rs328 | 0.732 | 0.440 | 8 | 19962213 | stop gained | C/G | snv | 9.2E-02 | 9.0E-02 | 7 | |
rs331 | 8 | 19962894 | intron variant | G/A | snv | 0.30 | 3 | ||||
rs12679834 | 8 | 19962922 | intron variant | T/C | snv | 9.4E-02 | 5 | ||||
rs10099160 | 8 | 19964304 | intron variant | T/G | snv | 0.20 | 2 | ||||
rs4922115 | 8 | 19965319 | 3 prime UTR variant | G/A | snv | 0.15 | 0.14 | 3 | |||
rs3289 | 8 | 19965681 | 3 prime UTR variant | T/C | snv | 4.0E-02 | 3 | ||||
rs11570892 | 8 | 19966106 | 3 prime UTR variant | A/G;T | snv | 3 | |||||
rs3208305 | 1.000 | 0.080 | 8 | 19966137 | 3 prime UTR variant | A/T | snv | 0.36 | 3 | ||
rs1059507 | 1.000 | 0.080 | 8 | 19966452 | 3 prime UTR variant | C/T | snv | 0.15 | 3 | ||
rs3735964 | 1.000 | 0.080 | 8 | 19966534 | 3 prime UTR variant | C/A | snv | 9.1E-02 | 4 | ||
rs3200218 | 8 | 19966560 | 3 prime UTR variant | A/G;T | snv | 3 | |||||
rs13702 | 0.925 | 0.160 | 8 | 19966981 | 3 prime UTR variant | T/A;C | snv | 3 | |||
rs15285 | 1.000 | 0.040 | 8 | 19967156 | 3 prime UTR variant | C/T | snv | 0.36 | 1 | ||
rs3916027 | 8 | 19967357 | downstream gene variant | G/A | snv | 0.31 | 3 | ||||
rs9644636 | 8 | 19967385 | downstream gene variant | T/A;G | snv | 3 | |||||
rs4921683 | 8 | 19967557 | downstream gene variant | T/A | snv | 0.14 | 3 |