rs615672
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs615672(C;C) |
Make rs615672(C;G) |
Make rs615672(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32606394 |
is a | snp |
is | mentioned by |
dbSNP | rs615672 |
dbSNP (classic) | rs615672 |
ClinGen | rs615672 |
ebi | rs615672 |
HLI | rs615672 |
Exac | rs615672 |
Gnomad | rs615672 |
Varsome | rs615672 |
LitVar | rs615672 |
Map | rs615672 |
PheGenI | rs615672 |
Biobank | rs615672 |
1000 genomes | rs615672 |
hgdp | rs615672 |
ensembl | rs615672 |
geneview | rs615672 |
scholar | rs615672 |
rs615672 | |
pharmgkb | rs615672 |
gwascentral | rs615672 |
openSNP | rs615672 |
23andMe | rs615672 |
SNPshot | rs615672 |
SNPdbe | rs615672 |
MSV3d | rs615672 |
GWAS Ctlg | rs615672 |
GMAF | 0.4692 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
Rs615672 | |
---|---|
PubMed | [PMID 17554300] |
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 20017963] Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis.
[PMID 20369022] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.
[PMID 23678157] Integrative analyses for functional mechanisms underlying associations for rheumatoid arthritis.