rs10917661

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs10917661(C;T)

Make rs10917661(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

161671427

Gene

FCGR2B

is a	snp
is	mentioned by
dbSNP	rs10917661
dbSNP (classic)	rs10917661
ClinGen	rs10917661
ebi	rs10917661
HLI	rs10917661
Exac	rs10917661
Gnomad	rs10917661
Varsome	rs10917661
LitVar	rs10917661
Map	rs10917661
PheGenI	rs10917661
Biobank	rs10917661
1000 genomes	rs10917661
hgdp	rs10917661
ensembl	rs10917661
geneview	rs10917661
scholar	rs10917661
google	rs10917661
pharmgkb	rs10917661
gwascentral	rs10917661
openSNP	rs10917661
23andMe	rs10917661
SNPshot	rs10917661
SNPdbe	rs10917661
MSV3d	rs10917661
GWAS Ctlg	rs10917661

Max Magnitude

0

?

(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 24586589 ] Functional fcgamma receptor polymorphisms are associated with human allergy