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rs267606760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606760(A;A)
Make rs267606760(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position133636672
GeneDBH
is asnp
is mentioned by
dbSNPrs267606760
ebirs267606760
HLIrs267606760
Exacrs267606760
Varsomers267606760
Maprs267606760
PheGenIrs267606760
hapmaprs267606760
1000 genomesrs267606760
hgdprs267606760
ensemblrs267606760
gopubmedrs267606760
geneviewrs267606760
scholarrs267606760
googlers267606760
pharmgkbrs267606760
gwascentralrs267606760
openSNPrs267606760
23andMers267606760
23andMe allrs267606760
SNP Nexus

SNPshotrs267606760
SNPdbers267606760
MSV3drs267606760
GWAS Ctlgrs267606760
Max Magnitude0
ClinVar
Risk rs267606760(A;A)
Alt rs267606760(A;A)
Reference rs267606760(G;G)
Significance Pathogenic
Disease Dopamine beta hydroxylase deficiency
Variation info
Gene DBH
CLNDBN Dopamine beta hydroxylase deficiency
Reversed 0
HGVS NC_000009.11:g.136501794G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001822.2, RCV000201816.1,