rs267196
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs267196(A;A) |
| Make rs267196(A;T) |
| Make rs267196(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 7849102 |
| Gene | BMP6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs267196 |
| dbSNP (classic) | rs267196 |
| ClinGen | rs267196 |
| ebi | rs267196 |
| HLI | rs267196 |
| Exac | rs267196 |
| Gnomad | rs267196 |
| Varsome | rs267196 |
| LitVar | rs267196 |
| Map | rs267196 |
| PheGenI | rs267196 |
| Biobank | rs267196 |
| 1000 genomes | rs267196 |
| hgdp | rs267196 |
| ensembl | rs267196 |
| geneview | rs267196 |
| scholar | rs267196 |
| rs267196 | |
| pharmgkb | rs267196 |
| gwascentral | rs267196 |
| openSNP | rs267196 |
| 23andMe | rs267196 |
| SNPshot | rs267196 |
| SNPdbe | rs267196 |
| MSV3d | rs267196 |
| GWAS Ctlg | rs267196 |
| GMAF | 0.4555 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
Part of a haplotype linked to stroke affecting perhaps 5% of sickle cell anemia patients
[PMID 15784727
] Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.
[PMID 18187665] Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.
[PMID 20401335] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
