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rs76714703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs76714703(C;C)
Make rs76714703(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161629903
GeneFCGR3B
is asnp
is mentioned by
dbSNPrs76714703
ebirs76714703
HLIrs76714703
Exacrs76714703
Varsomers76714703
Maprs76714703
PheGenIrs76714703
hapmaprs76714703
1000 genomesrs76714703
hgdprs76714703
ensemblrs76714703
gopubmedrs76714703
geneviewrs76714703
scholarrs76714703
googlers76714703
pharmgkbrs76714703
gwascentralrs76714703
openSNPrs76714703
23andMers76714703
23andMe allrs76714703
SNP Nexus

SNPshotrs76714703
SNPdbers76714703
MSV3drs76714703
GWAS Ctlgrs76714703
Max Magnitude0
ClinVar
Risk rs76714703(C;C)
Alt rs76714703(C;C)
Reference rs76714703(T;T)
Significance Pathogenic
Disease Neutrophil-specific antigens na1/na2
Variation info
Gene FCGR3B
CLNDBN Neutrophil-specific antigens na1/na2
Reversed 0
HGVS NC_000001.11:g.161629903T>C
CLNSRC ClinVar OMIM Allelic Variant
CLNACC RCV000030607.1,