Source: GWASDB ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2844511 | 0.807 | 0.200 | 6 | 31422007 | intron variant | A/G;T | snv | 7 | |||
rs9261290 | 0.807 | 0.280 | 6 | 30070870 | 3 prime UTR variant | T/C;G | snv | 5.2E-02; 7.2E-06 | 10 | ||
rs13194504 | 0.925 | 0.120 | 6 | 28662914 | intergenic variant | G/A | snv | 5.1E-02 | 2 | ||
rs3117143 | 0.882 | 0.160 | 6 | 29063365 | intron variant | C/A | snv | 5.2E-02 | 4 | ||
rs3749971 | 0.925 | 0.160 | 6 | 29374998 | missense variant | G/A | snv | 5.5E-02 | 5.7E-02 | 3 | |
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 11 | |
rs1235162 | 0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 | 6 | ||
rs3130380 | 0.807 | 0.280 | 6 | 30311353 | intron variant | G/A | snv | 6.6E-02 | 10 | ||
rs3131093 | 0.925 | 0.160 | 6 | 28869660 | intergenic variant | C/T | snv | 7.1E-02 | 3 | ||
rs4324798 | 0.790 | 0.240 | 6 | 28808340 | intergenic variant | G/A | snv | 7.2E-02 | 5 | ||
rs1233579 | 0.925 | 0.160 | 6 | 28744886 | intergenic variant | A/G | snv | 7.2E-02 | 3 |