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rs10127939

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 1 immunodeficiency, but not for 23andMe users
(T;T) 0 common in clinvar
Make rs10127939(A;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position161548543
GeneFCGR3A
is asnp
is mentioned by
dbSNPrs10127939
ebirs10127939
HLIrs10127939
Exacrs10127939
Varsomers10127939
Maprs10127939
PheGenIrs10127939
hapmaprs10127939
1000 genomesrs10127939
hgdprs10127939
ensemblrs10127939
gopubmedrs10127939
geneviewrs10127939
scholarrs10127939
googlers10127939
pharmgkbrs10127939
gwascentralrs10127939
openSNPrs10127939
23andMers10127939
23andMe allrs10127939
SNP Nexus

SNPshotrs10127939
SNPdbers10127939
MSV3drs10127939
GWAS Ctlgrs10127939
GMAF0.03581
Max Magnitude1
OMIM146740
Desc
Variant0002
Relatedalso
? (A;A) (A;C) (C;C)


ClinVar
Risk Rs10127939(A;A) rs10127939(G;G)
Alt Rs10127939(A;A) rs10127939(G;G)
Reference Rs10127939(T;T)
Significance Pathogenic
Disease Immunodeficiency 20
Variation info
Gene FCGR3A
CLNDBN Immunodeficiency 20
Reversed 1
HGVS NC_000001.10:g.161518333A>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000015953.3,



[PMID 24375423] FcγRIIIa SNPs and haplotypes affect human IgG binding and association with lupus nephritis in African Americans


[PMID 24782186OA-icon.png] Fcγ Receptor IIIa Single-Nucleotide Polymorphisms and Haplotypes Affect Human IgG Binding and Are Associated With Lupus Nephritis in African Americans