rs2274567
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2274567(A;A) |
| Make rs2274567(A;G) |
| Make rs2274567(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 207580276 |
| Gene | CR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2274567 |
| dbSNP (classic) | rs2274567 |
| ClinGen | rs2274567 |
| ebi | rs2274567 |
| HLI | rs2274567 |
| Exac | rs2274567 |
| Gnomad | rs2274567 |
| Varsome | rs2274567 |
| LitVar | rs2274567 |
| Map | rs2274567 |
| PheGenI | rs2274567 |
| Biobank | rs2274567 |
| 1000 genomes | rs2274567 |
| hgdp | rs2274567 |
| ensembl | rs2274567 |
| geneview | rs2274567 |
| scholar | rs2274567 |
| rs2274567 | |
| pharmgkb | rs2274567 |
| gwascentral | rs2274567 |
| openSNP | rs2274567 |
| 23andMe | rs2274567 |
| SNPshot | rs2274567 |
| SNPdbe | rs2274567 |
| MSV3d | rs2274567 |
| GWAS Ctlg | rs2274567 |
| GMAF | 0.2227 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 24018213] Missense variants in CR1 are associated with increased risk of Alzheimer' disease in Han Chinese
[PMID 21347408
] Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease.
[PMID 21700265] Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.
[PMID 25494101] Correlation of ECR1 A3650G Polymorphism with Neonatal Respiratory Distress Syndrome
[PMID 25683978] Association of the single-nucleotide polymorphism and haplotype of the complement receptor 1 gene with malaria
