rs408505
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs408505(C;C) |
| Make rs408505(C;T) |
| Make rs408505(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 7866194 |
| Gene | BMP6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs408505 |
| dbSNP (classic) | rs408505 |
| ClinGen | rs408505 |
| ebi | rs408505 |
| HLI | rs408505 |
| Exac | rs408505 |
| Gnomad | rs408505 |
| Varsome | rs408505 |
| LitVar | rs408505 |
| Map | rs408505 |
| PheGenI | rs408505 |
| Biobank | rs408505 |
| 1000 genomes | rs408505 |
| hgdp | rs408505 |
| ensembl | rs408505 |
| geneview | rs408505 |
| scholar | rs408505 |
| rs408505 | |
| pharmgkb | rs408505 |
| gwascentral | rs408505 |
| openSNP | rs408505 |
| 23andMe | rs408505 |
| SNPshot | rs408505 |
| SNPdbe | rs408505 |
| MSV3d | rs408505 |
| GWAS Ctlg | rs408505 |
| GMAF | 0.4174 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 20401335] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
