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rs863225245

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225245(G;T)
Make rs863225245(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position133643474
GeneDBH
is asnp
is mentioned by
dbSNPrs863225245
ebirs863225245
HLIrs863225245
Exacrs863225245
Varsomers863225245
Maprs863225245
PheGenIrs863225245
hapmaprs863225245
1000 genomesrs863225245
hgdprs863225245
ensemblrs863225245
gopubmedrs863225245
geneviewrs863225245
scholarrs863225245
googlers863225245
pharmgkbrs863225245
gwascentralrs863225245
openSNPrs863225245
23andMers863225245
23andMe allrs863225245
SNP Nexus

SNPshotrs863225245
SNPdbers863225245
MSV3drs863225245
GWAS Ctlgrs863225245
Max Magnitude0
ClinVar
Risk rs863225245(T;T)
Alt rs863225245(T;T)
Reference rs863225245(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.136508596G>T
CLNSRC
CLNACC RCV000201835.1,