Have questions? Visit https://www.reddit.com/r/SNPedia

rs193922450

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922450(C;T)
Make rs193922450(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position37782108
GeneCYBB
is asnp
is mentioned by
dbSNPrs193922450
ebirs193922450
HLIrs193922450
Exacrs193922450
Varsomers193922450
Maprs193922450
PheGenIrs193922450
hapmaprs193922450
1000 genomesrs193922450
hgdprs193922450
ensemblrs193922450
gopubmedrs193922450
geneviewrs193922450
scholarrs193922450
googlers193922450
pharmgkbrs193922450
gwascentralrs193922450
openSNPrs193922450
23andMers193922450
23andMe allrs193922450
SNP Nexus

SNPshotrs193922450
SNPdbers193922450
MSV3drs193922450
GWAS Ctlgrs193922450
Max Magnitude0
ClinVar
Risk rs193922450(T;T)
Alt rs193922450(T;T)
Reference rs193922450(C;C)
Significance Probable-Pathogenic
Disease Chronic granulomatous disease
Variation info
Gene CYBB
CLNDBN Chronic granulomatous disease, X-linked
Reversed 0
HGVS NC_000023.10:g.37641361C>A; NC_000023.10:g.37641361C>T
CLNSRC
CLNACC RCV000190516.1, RCV000029632.1,