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rs74853476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs74853476(C;C)
Make rs74853476(C;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position133636712
GeneDBH
is asnp
is mentioned by
dbSNPrs74853476
ebirs74853476
HLIrs74853476
Exacrs74853476
Varsomers74853476
Maprs74853476
PheGenIrs74853476
hapmaprs74853476
1000 genomesrs74853476
hgdprs74853476
ensemblrs74853476
gopubmedrs74853476
geneviewrs74853476
scholarrs74853476
googlers74853476
pharmgkbrs74853476
gwascentralrs74853476
openSNPrs74853476
23andMers74853476
23andMe allrs74853476
SNP Nexus

SNPshotrs74853476
SNPdbers74853476
MSV3drs74853476
GWAS Ctlgrs74853476
Max Magnitude0
ClinVar
Risk rs74853476(C;C)
Alt rs74853476(C;C)
Reference rs74853476(T;T)
Significance Pathogenic
Disease Dopamine beta hydroxylase deficiency
Variation info
Gene DBH
CLNDBN Dopamine beta hydroxylase deficiency
Reversed 0
HGVS NC_000009.11:g.136501834T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001820.4,