rs3766379
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | normal |
(C;T) | 1.37x increased risk for rheumatoid arthritis | |
(T;T) | 1.9x increased risk for rheumatoid arthritis |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 160837925 |
Gene | CD244 |
is a | snp |
is | mentioned by |
dbSNP | rs3766379 |
dbSNP (classic) | rs3766379 |
ClinGen | rs3766379 |
ebi | rs3766379 |
HLI | rs3766379 |
Exac | rs3766379 |
Gnomad | rs3766379 |
Varsome | rs3766379 |
LitVar | rs3766379 |
Map | rs3766379 |
PheGenI | rs3766379 |
Biobank | rs3766379 |
1000 genomes | rs3766379 |
hgdp | rs3766379 |
ensembl | rs3766379 |
geneview | rs3766379 |
scholar | rs3766379 |
rs3766379 | |
pharmgkb | rs3766379 |
gwascentral | rs3766379 |
openSNP | rs3766379 |
23andMe | rs3766379 |
SNPshot | rs3766379 |
SNPdbe | rs3766379 |
MSV3d | rs3766379 |
GWAS Ctlg | rs3766379 |
GMAF | 0.4656 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Two SNPs on ch 1q in the CD244 gene, rs3766379 and rs6682654, were found to be associated with risk for rheumatoid arthritis in two independent Japanese cohorts (p = 3.23 x 10e-8) and p = 7.45 x 10e-8). The odds ratio reported for the more common rs3766379(T) allele was 1.37 (CI: 1.18-1.59, p = 0.0001).[PMID 18794858]
[PMID 20437071] Single nucleotide polymorphisms of CD244 gene predispose to renal and neuropsychiatric manifestations with systemic lupus erythematosus.
ClinVar | |
---|---|
Risk | Rs3766379(C;C) |
Alt | Rs3766379(C;C) |
Reference | Rs3766379(T;T) |
Significance | Other |
Disease | Rheumatoid arthritis |
Variation | info |
Gene | CD244 |
CLNDBN | Rheumatoid arthritis |
Reversed | 0 |
HGVS | NC_000001.10:g.160807715T>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000005173.2, |