Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3132580 | 0.790 | 0.360 | 6 | 30952347 | missense variant | G/A | snv | 8.0E-02 | 9.3E-02 | 6 | |
rs3132610 | 0.807 | 0.280 | 6 | 30576624 | intron variant | A/G | snv | 7.4E-02 | 5 | ||
rs3132685 | 0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv | 5 | |||
rs3134942 | 0.790 | 0.320 | 6 | 32200994 | synonymous variant | G/T | snv | 9.7E-02 | 0.11 | 6 | |
rs389884 | 0.776 | 0.440 | 6 | 31973120 | non coding transcript exon variant | A/G | snv | 7.1E-02 | 7 | ||
rs558702 | 0.807 | 0.320 | 6 | 31902549 | intron variant | G/A | snv | 7.7E-02 | 6 | ||
rs7750641 | 0.807 | 0.360 | 6 | 31161533 | missense variant | C/T | snv | 7.0E-02 | 7.6E-02 | 5 | |
rs7762279 | 0.807 | 0.360 | 6 | 32787513 | intergenic variant | T/C | snv | 8.4E-02 | 6 | ||
rs7775397 | 0.790 | 0.400 | 6 | 32293475 | missense variant | T/G | snv | 6.0E-02 | 6.4E-02 | 6 | |
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 11 | |
rs886424 | 0.776 | 0.320 | 6 | 30814225 | non coding transcript exon variant | C/T | snv | 7.1E-02 | 8.7E-02 | 7 | |
rs9261290 | 0.807 | 0.280 | 6 | 30070870 | 3 prime UTR variant | T/C;G | snv | 5.2E-02; 7.2E-06 | 10 | ||
rs9262143 | 0.851 | 0.240 | 6 | 30685004 | missense variant | C/G;T | snv | 4.1E-06; 6.1E-02 | 4 |