rs3737002
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3737002(C;C) |
| Make rs3737002(C;T) |
| Make rs3737002(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 207587428 |
| Gene | CR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3737002 |
| dbSNP (classic) | rs3737002 |
| ClinGen | rs3737002 |
| ebi | rs3737002 |
| HLI | rs3737002 |
| Exac | rs3737002 |
| Gnomad | rs3737002 |
| Varsome | rs3737002 |
| LitVar | rs3737002 |
| Map | rs3737002 |
| PheGenI | rs3737002 |
| Biobank | rs3737002 |
| 1000 genomes | rs3737002 |
| hgdp | rs3737002 |
| ensembl | rs3737002 |
| geneview | rs3737002 |
| scholar | rs3737002 |
| rs3737002 | |
| pharmgkb | rs3737002 |
| gwascentral | rs3737002 |
| openSNP | rs3737002 |
| 23andMe | rs3737002 |
| SNPshot | rs3737002 |
| SNPdbe | rs3737002 |
| MSV3d | rs3737002 |
| GWAS Ctlg | rs3737002 |
| GMAF | 0.2658 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24018213] Missense variants in CR1 are associated with increased risk of Alzheimer' disease in Han Chinese
[PMID 29920840] Targeted resequencing reveals genetic risks in patients with sporadic idiopathic pulmonary fibrosis.
