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