Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2516400 | 0.827 | 0.320 | 6 | 31513328 | upstream gene variant | G/A | snv | 0.32 | 8 | ||
rs3130618 | 0.827 | 0.360 | 6 | 31664357 | missense variant | C/A;T | snv | 0.15; 4.0E-06 | 7 | ||
rs3132580 | 0.790 | 0.360 | 6 | 30952347 | missense variant | G/A | snv | 8.0E-02 | 9.3E-02 | 7 | |
rs9277534 | 0.790 | 0.280 | 6 | 33087030 | 3 prime UTR variant | A/G | snv | 0.38 | 7 | ||
rs3115663 | 0.827 | 0.360 | 6 | 31634066 | non coding transcript exon variant | T/C | snv | 0.17 | 7 | ||
rs3130564 | 0.790 | 0.360 | 6 | 31133897 | intron variant | C/T | snv | 0.14 | 7 | ||
rs4958881 | 0.827 | 0.280 | 5 | 151070675 | intron variant | T/C | snv | 0.21 | 7 | ||
rs7775397 | 0.790 | 0.400 | 6 | 32293475 | missense variant | T/G | snv | 6.0E-02 | 6.4E-02 | 7 | |
rs1794282 | 0.807 | 0.320 | 6 | 32698749 | intergenic variant | C/T | snv | 6.4E-02 | 6 | ||
rs3094054 | 0.807 | 0.280 | 6 | 30365728 | upstream gene variant | G/A;T | snv | 6 | |||
rs3130473 | 0.882 | 0.160 | 6 | 31231431 | intergenic variant | C/T | snv | 0.23 | 6 | ||
rs7762279 | 0.807 | 0.360 | 6 | 32787513 | intergenic variant | T/C | snv | 8.4E-02 | 6 | ||
rs3132610 | 0.807 | 0.280 | 6 | 30576624 | intron variant | A/G | snv | 7.4E-02 | 6 | ||
rs558702 | 0.807 | 0.320 | 6 | 31902549 | intron variant | G/A | snv | 7.7E-02 | 6 | ||
rs1235162 | 0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 | 6 | ||
rs3132685 | 0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv | 6 | |||
rs3131296 | 0.807 | 0.320 | 6 | 32205216 | intron variant | C/T | snv | 0.11 | 6 | ||
rs11229 | 0.851 | 0.280 | 6 | 31635993 | synonymous variant | A/G | snv | 0.14 | 0.17 | 6 | |
rs7750641 | 0.807 | 0.360 | 6 | 31161533 | missense variant | C/T | snv | 7.0E-02 | 7.6E-02 | 6 | |
rs3129890 | 0.827 | 0.280 | 6 | 32446496 | downstream gene variant | T/A;C | snv | 5 | |||
rs3130350 | 0.827 | 0.280 | 6 | 30360062 | upstream gene variant | G/T | snv | 7.1E-02 | 5 | ||
rs2524005 | 0.882 | 0.160 | 6 | 29931900 | upstream gene variant | G/A | snv | 0.18 | 5 | ||
rs2233956 | 0.827 | 0.320 | 6 | 31113428 | upstream gene variant | T/C | snv | 0.12 | 5 | ||
rs2523987 | 0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 | 5 | ||
rs2523989 | 0.827 | 0.280 | 6 | 30110498 | missense variant | C/T | snv | 0.12 | 0.12 | 5 |