rs284875
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs284875(A;A) |
| Make rs284875(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 91705151 |
| Gene | TGFBR3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs284875 |
| dbSNP (classic) | rs284875 |
| ClinGen | rs284875 |
| ebi | rs284875 |
| HLI | rs284875 |
| Exac | rs284875 |
| Gnomad | rs284875 |
| Varsome | rs284875 |
| LitVar | rs284875 |
| Map | rs284875 |
| PheGenI | rs284875 |
| Biobank | rs284875 |
| 1000 genomes | rs284875 |
| hgdp | rs284875 |
| ensembl | rs284875 |
| geneview | rs284875 |
| scholar | rs284875 |
| rs284875 | |
| pharmgkb | rs284875 |
| gwascentral | rs284875 |
| openSNP | rs284875 |
| 23andMe | rs284875 |
| SNPshot | rs284875 |
| SNPdbe | rs284875 |
| MSV3d | rs284875 |
| GWAS Ctlg | rs284875 |
| GMAF | 0.101 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Part of a haplotype linked to stroke affecting perhaps 5% of sickle cell anemia patients
[PMID 20401335
] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
