rs7527798
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7527798(C;C) |
| Make rs7527798(C;T) |
| Make rs7527798(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 207698945 |
| Gene | CR1L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7527798 |
| dbSNP (classic) | rs7527798 |
| ClinGen | rs7527798 |
| ebi | rs7527798 |
| HLI | rs7527798 |
| Exac | rs7527798 |
| Gnomad | rs7527798 |
| Varsome | rs7527798 |
| LitVar | rs7527798 |
| Map | rs7527798 |
| PheGenI | rs7527798 |
| Biobank | rs7527798 |
| 1000 genomes | rs7527798 |
| hgdp | rs7527798 |
| ensembl | rs7527798 |
| geneview | rs7527798 |
| scholar | rs7527798 |
| rs7527798 | |
| pharmgkb | rs7527798 |
| gwascentral | rs7527798 |
| openSNP | rs7527798 |
| 23andMe | rs7527798 |
| SNPshot | rs7527798 |
| SNPdbe | rs7527798 |
| MSV3d | rs7527798 |
| GWAS Ctlg | rs7527798 |
| GMAF | 0.141 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21700265 ]
|
| Trait | |
| Title | Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. |
| Risk Allele | |
| P-val | 2E-9 |
| Odds Ratio | 0.1000 [NR] unit increase |
[PMID 22430674] Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.
[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.
