rs6691117
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6691117(A;A) |
| Make rs6691117(A;G) |
| Make rs6691117(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 207609586 |
| Gene | CR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6691117 |
| dbSNP (classic) | rs6691117 |
| ClinGen | rs6691117 |
| ebi | rs6691117 |
| HLI | rs6691117 |
| Exac | rs6691117 |
| Gnomad | rs6691117 |
| Varsome | rs6691117 |
| LitVar | rs6691117 |
| Map | rs6691117 |
| PheGenI | rs6691117 |
| Biobank | rs6691117 |
| 1000 genomes | rs6691117 |
| hgdp | rs6691117 |
| ensembl | rs6691117 |
| geneview | rs6691117 |
| scholar | rs6691117 |
| rs6691117 | |
| pharmgkb | rs6691117 |
| gwascentral | rs6691117 |
| openSNP | rs6691117 |
| 23andMe | rs6691117 |
| SNPshot | rs6691117 |
| SNPdbe | rs6691117 |
| MSV3d | rs6691117 |
| GWAS Ctlg | rs6691117 |
| GMAF | 0.3893 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23591632
] Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth
[PMID 24018213] Missense variants in CR1 are associated with increased risk of Alzheimer' disease in Han Chinese
[PMID 21700265] Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.
[PMID 23856853] Association of a complement receptor 1 gene variant with baseline erythrocyte sedimentation rate levels in patients starting anti-TNF therapy in a UK rheumatoid arthritis cohort: results from the Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate cohort.
[PMID 26680604] Polygenic Analysis of Late-Onset Alzheimer's Disease from Mainland China.
