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rs448740

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 0.5 one of the differences in NA1 and NA2 neutrophil alloantigens
(T;T) 0 common in clinvar


Make rs448740(C;C)
ReferenceGRCh38 38.1/142
Chromosome1
Position161629903
GeneFCGR3B
is asnp
is mentioned by
dbSNPrs448740
ebirs448740
HLIrs448740
Exacrs448740
Varsomers448740
Maprs448740
PheGenIrs448740
hapmaprs448740
1000 genomesrs448740
hgdprs448740
ensemblrs448740
gopubmedrs448740
geneviewrs448740
scholarrs448740
googlers448740
pharmgkbrs448740
gwascentralrs448740
openSNPrs448740
23andMers448740
23andMe allrs448740
SNP Nexus

SNPshotrs448740
SNPdbers448740
MSV3drs448740
GWAS Ctlgrs448740
Max Magnitude0.5
? (C;C) (C;T) (T;T) 28


ClinVar
Risk rs448740(C;C)
Alt rs448740(C;C)
Reference rs448740(T;T)
Significance Pathogenic
Disease Neutrophil-specific antigens na1/na2
Variation info
Gene FCGR3B
CLNDBN Neutrophil-specific antigens na1/na2
Reversed 0
HGVS NC_000001.10:g.161599693T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000030607.2,