rs10506645
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10506645(C;C) |
Make rs10506645(C;T) |
Make rs10506645(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 71991720 |
Gene | TPH2 |
is a | snp |
is | mentioned by |
dbSNP | rs10506645 |
dbSNP (classic) | rs10506645 |
ClinGen | rs10506645 |
ebi | rs10506645 |
HLI | rs10506645 |
Exac | rs10506645 |
Gnomad | rs10506645 |
Varsome | rs10506645 |
LitVar | rs10506645 |
Map | rs10506645 |
PheGenI | rs10506645 |
Biobank | rs10506645 |
1000 genomes | rs10506645 |
hgdp | rs10506645 |
ensembl | rs10506645 |
geneview | rs10506645 |
scholar | rs10506645 |
rs10506645 | |
pharmgkb | rs10506645 |
gwascentral | rs10506645 |
openSNP | rs10506645 |
23andMe | rs10506645 |
SNPshot | rs10506645 |
SNPdbe | rs10506645 |
MSV3d | rs10506645 |
GWAS Ctlg | rs10506645 |
GMAF | 0.2893 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19800079] Association of polymorphisms of the tryptophan hydroxylase 2 gene with risk for bipolar disorder or suicidal behavior
[PMID 22698518] Melatonin pathway genes are associated with progressive subtypes and disability status in multiple sclerosis among Finnish patients
[PMID 19184136] Examination of association of genes in the serotonin system to autism.
[PMID 21085052] Association study of tryptophan hydroxylase 2 gene polymorphisms in bipolar disorder patients with panic disorder comorbidity.
[PMID 21412658] Associations between polymorphic variants of the tryptophan hydroxylase 2 gene and obsessive-compulsive disorder.