rs78162420

Orientation

plus

Stabilized

plus

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

Make rs78162420(A;A)

Make rs78162420(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

71941600

Gene

TPH2

is a	snp
is	mentioned by
dbSNP	rs78162420
dbSNP (classic)	rs78162420
ClinGen	rs78162420
ebi	rs78162420
HLI	rs78162420
Exac	rs78162420
Gnomad	rs78162420
Varsome	rs78162420
LitVar	rs78162420
Map	rs78162420
PheGenI	rs78162420
Biobank	rs78162420
1000 genomes	rs78162420
hgdp	rs78162420
ensembl	rs78162420
geneview	rs78162420
scholar	rs78162420
google	rs78162420
pharmgkb	rs78162420
gwascentral	rs78162420
openSNP	rs78162420
23andMe	rs78162420
SNPshot	rs78162420
SNPdbe	rs78162420
MSV3d	rs78162420
GWAS Ctlg	rs78162420

Max Magnitude

0

[PMID 28320136] Association between gene polymorphism and depression in Parkinson's disease: A case-control study.

ClinVar
Risk	rs78162420(A;A)
Alt	rs78162420(A;A)
Reference	Rs78162420(C;C)
Significance	Probable-non-pathogenic
Disease	Tryptophan 5-monooxygenase deficiency
Variation	info
Gene	TPH2
CLNDBN	Tryptophan 5-monooxygenase deficiency
Reversed	0
HGVS	NC_000012.11:g.72335380C>A
CLNSRC
CLNACC	RCV000334080.1,