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rs2290834

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2290834(C;C)
Make rs2290834(C;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position161629781
GeneFCGR3B
is asnp
is mentioned by
dbSNPrs2290834
ebirs2290834
HLIrs2290834
Exacrs2290834
Varsomers2290834
Maprs2290834
PheGenIrs2290834
hapmaprs2290834
1000 genomesrs2290834
hgdprs2290834
ensemblrs2290834
gopubmedrs2290834
geneviewrs2290834
scholarrs2290834
googlers2290834
pharmgkbrs2290834
gwascentralrs2290834
openSNPrs2290834
23andMers2290834
23andMe allrs2290834
SNP Nexus

SNPshotrs2290834
SNPdbers2290834
MSV3drs2290834
GWAS Ctlgrs2290834
Max Magnitude0
ClinVar
Risk rs2290834(C;C)
Alt rs2290834(C;C)
Reference rs2290834(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.161599571T\x3d
CLNSRC OMIM Allelic Variant
CLNACC RCV000030607.2,