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rs945635

From SNPedia

Orientationplus
Stabilizedplus
Make rs945635(C;C)
Make rs945635(C;G)
Make rs945635(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position157700500
GeneFCRL3
is asnp
is mentioned by
dbSNPrs945635
ebirs945635
HLIrs945635
Exacrs945635
Varsomers945635
Maprs945635
PheGenIrs945635
hapmaprs945635
1000 genomesrs945635
hgdprs945635
ensemblrs945635
gopubmedrs945635
geneviewrs945635
scholarrs945635
googlers945635
pharmgkbrs945635
gwascentralrs945635
openSNPrs945635
23andMers945635
23andMe allrs945635
SNP Nexus

SNPshotrs945635
SNPdbers945635
MSV3drs945635
GWAS Ctlgrs945635
GMAF0.4444
Max Magnitude
? (C;C) (C;G) (G;G) 28

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


[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 19877046OA-icon.png] The FCRL3-169CT promoter single-nucleotide polymorphism, which is associated with systemic lupus erythematosus in a Japanese population, predicts expression of receptor protein on CD19+ B cells.


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