rs863225244

Orientation

plus

Stabilized

plus

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

Make rs863225244(-;-)

Make rs863225244(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

133642337

Gene

DBH

is a	snp
is	mentioned by
dbSNP	rs863225244
dbSNP (classic)	rs863225244
ClinGen	rs863225244
ebi	rs863225244
HLI	rs863225244
Exac	rs863225244
Gnomad	rs863225244
Varsome	rs863225244
LitVar	rs863225244
Map	rs863225244
PheGenI	rs863225244
Biobank	rs863225244
1000 genomes	rs863225244
hgdp	rs863225244
ensembl	rs863225244
geneview	rs863225244
scholar	rs863225244
google	rs863225244
pharmgkb	rs863225244
gwascentral	rs863225244
openSNP	rs863225244
23andMe	rs863225244
SNPshot	rs863225244
SNPdbe	rs863225244
MSV3d	rs863225244
GWAS Ctlg	rs863225244

Max Magnitude

0

ClinVar
Risk	rs863225244(-;-)
Alt	rs863225244(-;-)
Reference	Rs863225244(A;A)
Significance	Pathogenic
Disease	Dopamine beta hydroxylase deficiency
Variation	info
Gene	DBH
CLNDBN	Dopamine beta hydroxylase deficiency
Reversed	0
HGVS	NC_000009.11:g.136507459delA
CLNSRC
CLNACC	RCV000201827.1,