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rs147574249

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs147574249(C;C)
Make rs147574249(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161629853
GeneFCGR3B
is asnp
is mentioned by
dbSNPrs147574249
ebirs147574249
HLIrs147574249
Exacrs147574249
Varsomers147574249
Maprs147574249
PheGenIrs147574249
hapmaprs147574249
1000 genomesrs147574249
hgdprs147574249
ensemblrs147574249
gopubmedrs147574249
geneviewrs147574249
scholarrs147574249
googlers147574249
pharmgkbrs147574249
gwascentralrs147574249
openSNPrs147574249
23andMers147574249
23andMe allrs147574249
SNP Nexus

SNPshotrs147574249
SNPdbers147574249
MSV3drs147574249
GWAS Ctlgrs147574249
Max Magnitude0
ClinVar
Risk rs147574249(C;C)
Alt rs147574249(C;C)
Reference rs147574249(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.161599643T\x3d
CLNSRC OMIM Allelic Variant
CLNACC RCV000030607.2,