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rs193922446

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922446(-;-)
Make rs193922446(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position37780092
GeneCYBB
is asnp
is mentioned by
dbSNPrs193922446
ebirs193922446
HLIrs193922446
Exacrs193922446
Varsomers193922446
Maprs193922446
PheGenIrs193922446
hapmaprs193922446
1000 genomesrs193922446
hgdprs193922446
ensemblrs193922446
gopubmedrs193922446
geneviewrs193922446
scholarrs193922446
googlers193922446
pharmgkbrs193922446
gwascentralrs193922446
openSNPrs193922446
23andMers193922446
23andMe allrs193922446
SNP Nexus

SNPshotrs193922446
SNPdbers193922446
MSV3drs193922446
GWAS Ctlgrs193922446
Max Magnitude0
ClinVar
Risk rs193922446(;)
Alt rs193922446(;)
Reference rs193922446(T;T)
Significance Probable-Pathogenic
Disease Chronic granulomatous disease
Variation info
Gene CYBB
CLNDBN Chronic granulomatous disease, X-linked
Reversed 0
HGVS NC_000023.10:g.37639345delT
CLNSRC ClinVar LabCorp
CLNACC RCV000029625.1,