rs7026551
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7026551(A;A) |
| Make rs7026551(A;C) |
| Make rs7026551(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 120970855 |
| Gene | C5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7026551 |
| dbSNP (classic) | rs7026551 |
| ClinGen | rs7026551 |
| ebi | rs7026551 |
| HLI | rs7026551 |
| Exac | rs7026551 |
| Gnomad | rs7026551 |
| Varsome | rs7026551 |
| LitVar | rs7026551 |
| Map | rs7026551 |
| PheGenI | rs7026551 |
| Biobank | rs7026551 |
| 1000 genomes | rs7026551 |
| hgdp | rs7026551 |
| ensembl | rs7026551 |
| geneview | rs7026551 |
| scholar | rs7026551 |
| rs7026551 | |
| pharmgkb | rs7026551 |
| gwascentral | rs7026551 |
| openSNP | rs7026551 |
| 23andMe | rs7026551 |
| SNPshot | rs7026551 |
| SNPdbe | rs7026551 |
| MSV3d | rs7026551 |
| GWAS Ctlg | rs7026551 |
| GMAF | 0.2631 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| Rs7026551 | |
|---|---|
| PubMed | [PMID 17804836 |
| Affy Probeset | SNP_A-8509717 |
| Affy Orientation | same |
| On GW 5.0 | 0 |
| Alleles A/B | A/C |
| Ancestral | C |
| Population | |
| Allele | C |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.31 |
| Disease | Rheumatoid Arthritis (RA) |
rs7026551 increases susceptibility to Rheumatoid Arthritis 1.31 times for carriers of the C allele [PMID 17804836
]
[PMID 17880261
] A candidate gene approach identifies the TRAF1/C5 region as a risk factor for rheumatoid arthritis.
[PMID 19344414
] Risk of non-Hodgkin lymphoma in association with germline variation in complement genes.
[PMID 20018062
] Identification of genes and haplotypes that predict rheumatoid arthritis using random forests.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 9
- Has genotype
- Has population
- Has Report GE
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d
