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rs387906485

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906485(A;A)
Make rs387906485(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position37783600
GeneCYBB
is asnp
is mentioned by
dbSNPrs387906485
ebirs387906485
HLIrs387906485
Exacrs387906485
Varsomers387906485
Maprs387906485
PheGenIrs387906485
hapmaprs387906485
1000 genomesrs387906485
hgdprs387906485
ensemblrs387906485
gopubmedrs387906485
geneviewrs387906485
scholarrs387906485
googlers387906485
pharmgkbrs387906485
gwascentralrs387906485
openSNPrs387906485
23andMers387906485
23andMe allrs387906485
SNP Nexus

SNPshotrs387906485
SNPdbers387906485
MSV3drs387906485
GWAS Ctlgrs387906485
Max Magnitude0
ClinVar
Risk rs387906485(A,T;A,T)
Alt rs387906485(A,T;A,T)
Reference rs387906485(G;G)
Significance Pathogenic
Disease Chronic granulomatous disease
Variation info
Gene CYBB
CLNDBN Chronic granulomatous disease, X-linked
Reversed 0
HGVS NC_000023.10:g.37642853G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011680.5,