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rs193922448

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922448(C;C)
Make rs193922448(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position37793716
GeneCYBB
is asnp
is mentioned by
dbSNPrs193922448
ebirs193922448
HLIrs193922448
Exacrs193922448
Varsomers193922448
Maprs193922448
PheGenIrs193922448
hapmaprs193922448
1000 genomesrs193922448
hgdprs193922448
ensemblrs193922448
gopubmedrs193922448
geneviewrs193922448
scholarrs193922448
googlers193922448
pharmgkbrs193922448
gwascentralrs193922448
openSNPrs193922448
23andMers193922448
23andMe allrs193922448
SNP Nexus

SNPshotrs193922448
SNPdbers193922448
MSV3drs193922448
GWAS Ctlgrs193922448
Max Magnitude0
ClinVar
Risk rs193922448(C;C)
Alt rs193922448(C;C)
Reference rs193922448(G;G)
Significance Probable-Pathogenic
Disease Chronic granulomatous disease
Variation info
Gene CYBB
CLNDBN Chronic granulomatous disease, X-linked
Reversed 0
HGVS NC_000023.10:g.37652969G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029628.1,