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rs199890941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199890941(C;C)
Make rs199890941(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161629781
GeneFCGR3B
is asnp
is mentioned by
dbSNPrs199890941
ebirs199890941
HLIrs199890941
Exacrs199890941
Varsomers199890941
Maprs199890941
PheGenIrs199890941
hapmaprs199890941
1000 genomesrs199890941
hgdprs199890941
ensemblrs199890941
gopubmedrs199890941
geneviewrs199890941
scholarrs199890941
googlers199890941
pharmgkbrs199890941
gwascentralrs199890941
openSNPrs199890941
23andMers199890941
23andMe allrs199890941
SNP Nexus

SNPshotrs199890941
SNPdbers199890941
MSV3drs199890941
GWAS Ctlgrs199890941
Max Magnitude0
ClinVar
Risk rs199890941(C;C)
Alt rs199890941(C;C)
Reference rs199890941(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.161629781T\x3d
CLNSRC ClinVar OMIM Allelic Variant
CLNACC RCV000030607.1,