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rs7026551

From SNPedia

Orientationplus
Stabilizedplus
Make rs7026551(A;A)
Make rs7026551(A;C)
Make rs7026551(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position120970855
GeneC5
is asnp
is mentioned by
dbSNPrs7026551
ebirs7026551
HLIrs7026551
Exacrs7026551
Varsomers7026551
Maprs7026551
PheGenIrs7026551
hapmaprs7026551
1000 genomesrs7026551
hgdprs7026551
ensemblrs7026551
gopubmedrs7026551
geneviewrs7026551
scholarrs7026551
googlers7026551
pharmgkbrs7026551
gwascentralrs7026551
openSNPrs7026551
23andMers7026551
23andMe allrs7026551
SNP Nexus

SNPshotrs7026551
SNPdbers7026551
MSV3drs7026551
GWAS Ctlgrs7026551
GMAF0.2631
Max Magnitude
? (A;A) (A;C) (C;C) 28
Rs7026551
PubMed [PMID 17804836OA-icon.png]
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 17804836OA-icon.png]


[PMID 17880261OA-icon.png] A candidate gene approach identifies the TRAF1/C5 region as a risk factor for rheumatoid arthritis.


[PMID 19344414OA-icon.png] Risk of non-Hodgkin lymphoma in association with germline variation in complement genes.


[PMID 20018062OA-icon.png] Identification of genes and haplotypes that predict rheumatoid arthritis using random forests.