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rs3761959

From SNPedia

Orientationminus
Stabilizedminus
Make rs3761959(A;A)
Make rs3761959(A;G)
Make rs3761959(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position157699488
GeneFCRL3
is asnp
is mentioned by
dbSNPrs3761959
ebirs3761959
HLIrs3761959
Exacrs3761959
Varsomers3761959
Maprs3761959
PheGenIrs3761959
hapmaprs3761959
1000 genomesrs3761959
hgdprs3761959
ensemblrs3761959
gopubmedrs3761959
geneviewrs3761959
scholarrs3761959
googlers3761959
pharmgkbrs3761959
gwascentralrs3761959
openSNPrs3761959
23andMers3761959
23andMe allrs3761959
SNP Nexus

SNPshotrs3761959
SNPdbers3761959
MSV3drs3761959
GWAS Ctlgrs3761959
GMAF0.4995
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21841780]
Trait
Title A genome-wide association study identifies two new risk loci for Graves' disease.
Risk Allele A
P-val 2E-13
Odds Ratio 1.2300 [1.17-1.30]


[PMID 16859508OA-icon.png] Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?


[PMID 18556175] Lack of association between Fc receptor-like 3 gene polymorphisms and systemic lupus erythematosus in Chinese population.


[PMID 19050767OA-icon.png] Association between polymorphisms of FCRL3, a non-HLA gene, and Behcet's disease in a Chinese population with ophthalmic manifestations.


[PMID 19452015OA-icon.png] Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome.


[PMID 23505439OA-icon.png] A Refined Study of FCRL Genes from a Genome-Wide Association Study for Graves' Disease

GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait Multiple sclerosis
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele G
P-val 3E-6
Odds Ratio 1.08 [1.06-1.09]


[PMID 24117236] The Fc receptor-like 3 gene polymorphisms and susceptibility to autoimmune diseases: An updated meta-analysis


[PMID 26051414] FCRL3 gene polymorphisms confer risk for sudden sensorineural hearing loss in a Chinese Han Population