rs2869967
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2869967(C;C) |
| Make rs2869967(C;T) |
| Make rs2869967(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 88948181 |
| Gene | FAM13A, LOC105377327 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2869967 |
| dbSNP (classic) | rs2869967 |
| ClinGen | rs2869967 |
| ebi | rs2869967 |
| HLI | rs2869967 |
| Exac | rs2869967 |
| Gnomad | rs2869967 |
| Varsome | rs2869967 |
| LitVar | rs2869967 |
| Map | rs2869967 |
| PheGenI | rs2869967 |
| Biobank | rs2869967 |
| 1000 genomes | rs2869967 |
| hgdp | rs2869967 |
| ensembl | rs2869967 |
| geneview | rs2869967 |
| scholar | rs2869967 |
| rs2869967 | |
| pharmgkb | rs2869967 |
| gwascentral | rs2869967 |
| openSNP | rs2869967 |
| 23andMe | rs2869967 |
| SNPshot | rs2869967 |
| SNPdbe | rs2869967 |
| MSV3d | rs2869967 |
| GWAS Ctlg | rs2869967 |
| GMAF | 0.4968 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20010835 ]
|
| Trait | Pulmonary function |
| Title | Meta-analyses of genome-wide assocation studies identify multiple loci associated with pulmonary function |
| Risk Allele | T |
| P-val | 1E-7 |
| Odds Ratio | 0.30 [NR] % increase |
[PMID 20173748] Variants in FAM13A are associated with chronic obstructive pulmonary disease.
[PMID 22027142] Genetic analysis of IREB2, FAM13A and XRCC5 variants in Chinese Han patients with chronic obstructive pulmonary disease.
| GWAS snp | |
|---|---|
| PMID | [PMID 23284291]
|
| Trait | Pulmonary function (interaction) |
| Title | Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. |
| Risk Allele | |
| P-val | 5E-11 |
| Odds Ratio | NR NR |
[PMID 23891779] Association of FAM13A polymorphisms with COPD and COPD-related phenotypes in Han Chinese
