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rs137854592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854592(C;T)
Make rs137854592(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position37798956
GeneCYBB
is asnp
is mentioned by
dbSNPrs137854592
ebirs137854592
HLIrs137854592
Exacrs137854592
Varsomers137854592
Maprs137854592
PheGenIrs137854592
hapmaprs137854592
1000 genomesrs137854592
hgdprs137854592
ensemblrs137854592
gopubmedrs137854592
geneviewrs137854592
scholarrs137854592
googlers137854592
pharmgkbrs137854592
gwascentralrs137854592
openSNPrs137854592
23andMers137854592
23andMe allrs137854592
SNP Nexus

SNPshotrs137854592
SNPdbers137854592
MSV3drs137854592
GWAS Ctlgrs137854592
Max Magnitude0
OMIM300481
Desc
Variant0009
Relatedalso
ClinVar
Risk rs137854592(T;T)
Alt rs137854592(T;T)
Reference rs137854592(C;C)
Significance Pathogenic
Disease Chronic granulomatous disease
Variation info
Gene CYBB
CLNDBN Chronic granulomatous disease, X-linked
Reversed 0
HGVS NC_000023.10:g.37658209C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011676.9,