rs7671167
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7671167(C;C) |
| Make rs7671167(C;T) |
| Make rs7671167(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 88962828 |
| Gene | FAM13A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7671167 |
| dbSNP (classic) | rs7671167 |
| ClinGen | rs7671167 |
| ebi | rs7671167 |
| HLI | rs7671167 |
| Exac | rs7671167 |
| Gnomad | rs7671167 |
| Varsome | rs7671167 |
| LitVar | rs7671167 |
| Map | rs7671167 |
| PheGenI | rs7671167 |
| Biobank | rs7671167 |
| 1000 genomes | rs7671167 |
| hgdp | rs7671167 |
| ensembl | rs7671167 |
| geneview | rs7671167 |
| scholar | rs7671167 |
| rs7671167 | |
| pharmgkb | rs7671167 |
| gwascentral | rs7671167 |
| openSNP | rs7671167 |
| 23andMe | rs7671167 |
| SNPshot | rs7671167 |
| SNPdbe | rs7671167 |
| MSV3d | rs7671167 |
| GWAS Ctlg | rs7671167 |
| GMAF | 0.4858 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20173748 ]
|
| Trait | Chronic obstructive pulmonary disease |
| Title | Variants in FAM13A are associated with chronic obstructive pulmonary disease |
| Risk Allele | |
| P-val | 1E-11 |
| Odds Ratio | 1.32 [1.19-1.47] |
[PMID 21304900] Individual and cumulative effects of GWAS susceptibility loci in lung cancer: associations after sub-phenotyping for COPD.
[PMID 23891779] Association of FAM13A polymorphisms with COPD and COPD-related phenotypes in Han Chinese
[PMID 25154699] Phenotypic and genetic heterogeneity among subjects with mild airflow obstruction in COPDGene
[PMID 26251585] Variants in multiple genes polymorphism association analysis of COPD in the Chinese Li population
