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rs10917661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10917661(C;T)
Make rs10917661(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161671427
GeneFCGR2B
is asnp
is mentioned by
dbSNPrs10917661
ebirs10917661
HLIrs10917661
Exacrs10917661
Varsomers10917661
Maprs10917661
PheGenIrs10917661
hapmaprs10917661
1000 genomesrs10917661
hgdprs10917661
ensemblrs10917661
gopubmedrs10917661
geneviewrs10917661
scholarrs10917661
googlers10917661
pharmgkbrs10917661
gwascentralrs10917661
openSNPrs10917661
23andMers10917661
23andMe allrs10917661
SNP Nexus

SNPshotrs10917661
SNPdbers10917661
MSV3drs10917661
GWAS Ctlgrs10917661
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 22416796] The FCGR2B rs10917661 polymorphism may confer susceptibility to ankylosing spondylitis in Han Chinese: a case-control study [PMID 16531013] Association of Fcgamma receptor IIB gene polymorphism with genetic susceptibility to systemic lupus erythematosus in Chinese populations--a family-based association study.


[PMID 17393178] Gln50Ter polymorphism of Fcgamma receptor IIB gene associated with genetic susceptibility to human systemic lupus erythematosus in Chinese populations.


[PMID 18625651] Genetic susceptibility and haplotype analysis between Fcgamma receptor IIB and IIIA gene with systemic lupus erythematosus in Chinese population.

[PMID 24586589OA-icon.png] Functional fcgamma receptor polymorphisms are associated with human allergy