rs78162420
From SNPedia
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 |
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, |