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rs615672

From SNPedia

Orientationplus
Stabilizedplus
Make rs615672(C;C)
Make rs615672(C;G)
Make rs615672(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32606394
is asnp
is mentioned by
dbSNPrs615672
ebirs615672
HLIrs615672
Exacrs615672
Varsomers615672
Maprs615672
PheGenIrs615672
hapmaprs615672
1000 genomesrs615672
hgdprs615672
ensemblrs615672
gopubmedrs615672
geneviewrs615672
scholarrs615672
googlers615672
pharmgkbrs615672
gwascentralrs615672
openSNPrs615672
23andMers615672
23andMe allrs615672
SNP Nexus

SNPshotrs615672
SNPdbers615672
MSV3drs615672
GWAS Ctlgrs615672
GMAF0.4692
Max Magnitude
? (C;C) (C;G) (G;G) 28
Rs615672
PubMed [PMID 17554300OA-icon.png]
Affy Probeset SNP_A-1956213
Affy Orientation same
On GW 5.0 1
Alleles A/B C/G
Ancestral G
Population
Allele
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All
Disease Rheumatoid Arthritis (RA)


[PMID 20017963OA-icon.png] Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis.

[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


GET Evidence
rs615672
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.377193
summary



[PMID 23678157] Integrative analyses for functional mechanisms underlying associations for rheumatoid arthritis.