rs863225245

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs863225245(G;T)

Make rs863225245(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

133643474

Gene

DBH

is a	snp
is	mentioned by
dbSNP	rs863225245
dbSNP (classic)	rs863225245
ClinGen	rs863225245
ebi	rs863225245
HLI	rs863225245
Exac	rs863225245
Gnomad	rs863225245
Varsome	rs863225245
LitVar	rs863225245
Map	rs863225245
PheGenI	rs863225245
Biobank	rs863225245
1000 genomes	rs863225245
hgdp	rs863225245
ensembl	rs863225245
geneview	rs863225245
scholar	rs863225245
google	rs863225245
pharmgkb	rs863225245
gwascentral	rs863225245
openSNP	rs863225245
23andMe	rs863225245
SNPshot	rs863225245
SNPdbe	rs863225245
MSV3d	rs863225245
GWAS Ctlg	rs863225245

Max Magnitude

0

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,