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rs151344498

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151344498(A;C)
Make rs151344498(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position37798972
GeneCYBB
is asnp
is mentioned by
dbSNPrs151344498
ebirs151344498
HLIrs151344498
Exacrs151344498
Varsomers151344498
Maprs151344498
PheGenIrs151344498
hapmaprs151344498
1000 genomesrs151344498
hgdprs151344498
ensemblrs151344498
gopubmedrs151344498
geneviewrs151344498
scholarrs151344498
googlers151344498
pharmgkbrs151344498
gwascentralrs151344498
openSNPrs151344498
23andMers151344498
23andMe allrs151344498
SNP Nexus

SNPshotrs151344498
SNPdbers151344498
MSV3drs151344498
GWAS Ctlgrs151344498
Max Magnitude0
ClinVar
Risk rs151344498(C;C)
Alt rs151344498(C;C)
Reference rs151344498(A;A)
Significance Pathogenic
Disease Atypical mycobacteriosis not provided Chronic granulomatous disease
Variation info
Gene CYBB
CLNDBN Atypical mycobacteriosis, familial, X-linked 2 not provided Chronic granulomatous disease
Reversed 0
HGVS NC_000023.10:g.37658225A>C
CLNSRC OMIM Allelic Variant UniProtKB (variants)
CLNACC RCV000022861.7, RCV000059275.1, RCV000208611.1,