chr11:18047816:G>T Detail (hg19) (TPH1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:18,047,816-18,047,816 |
hg38 | chr11:18,026,269-18,026,269 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_004179.2:c.803+221C>A | |
Ensemble | ENST00000250018.6:c.803+221C>A | |
ENST00000682019.1:c.803+221C>A |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.488 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
Prediction
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.011 | Unipolar Depression | In this study, we evaluated the association of seven serotonin signal transducti... | BeFree | 19590397 | Detail |
0.155 | major depressive disorder | In this study, we evaluated the association of seven serotonin signal transducti... | BeFree | 19590397 | Detail |
0.004 | borderline personality disorder | [The tryptophan hydroxylase-1 A218C polymorphism is associated with diagnosis, b... | GAD | 18506706 | Detail |
0.017 | Mood Disorders | Three hundred and ninety-eight patients diagnosed with mood disorders were genot... | BeFree | 21989108 | Detail |
0.031 | major depressive disorder | Our aim was to assess the association of TPH1 A218C polymorphism (rs1800532) wit... | BeFree | 21601290 | Detail |
0.031 | major depressive disorder | The A allele at TPH1 rs1800532 may be associated with citalopram efficacy only i... | BeFree | 23221997 | Detail |
0.002 | Mental disorders | Three hundred and ninety-eight patients diagnosed with mood disorders were genot... | BeFree | 21989108 | Detail |
0.005 | Unipolar Depression | The A allele at TPH1 rs1800532 may be associated with citalopram efficacy only i... | BeFree | 23221997 | Detail |
0.001 | Ichthyosis bullosa of Siemens | However, TPH1 gene SNPs were associated with IBS-related cognitions (rs4537731 a... | BeFree | 23172723 | Detail |
0.005 | Unipolar Depression | Our aim was to assess the association of TPH1 A218C polymorphism (rs1800532) wit... | BeFree | 21601290 | Detail |
<0.001 | Drug habituation | According to this practical and scientific demand, we aimed to investigate the r... | BeFree | 20421849 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
In this study, we evaluated the association of seven serotonin signal transduction-linked single nuc... | DisGeNET | Detail |
In this study, we evaluated the association of seven serotonin signal transduction-linked single nuc... | DisGeNET | Detail |
[The tryptophan hydroxylase-1 A218C polymorphism is associated with diagnosis, but not suicidal beha... | DisGeNET | Detail |
Three hundred and ninety-eight patients diagnosed with mood disorders were genotyped for TPH1 G-6526... | DisGeNET | Detail |
Our aim was to assess the association of TPH1 A218C polymorphism (rs1800532) with mood disorders, in... | DisGeNET | Detail |
The A allele at TPH1 rs1800532 may be associated with citalopram efficacy only in melancholic and ps... | DisGeNET | Detail |
Three hundred and ninety-eight patients diagnosed with mood disorders were genotyped for TPH1 G-6526... | DisGeNET | Detail |
The A allele at TPH1 rs1800532 may be associated with citalopram efficacy only in melancholic and ps... | DisGeNET | Detail |
However, TPH1 gene SNPs were associated with IBS-related cognitions (rs4537731 and rs21105) and qual... | DisGeNET | Detail |
Our aim was to assess the association of TPH1 A218C polymorphism (rs1800532) with mood disorders, in... | DisGeNET | Detail |
According to this practical and scientific demand, we aimed to investigate the relationship between ... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs1800532 dbSNP
- Genome
- hg19
- Position
- chr11:18,047,816-18,047,816
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs1800532
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.4885
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 8186
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16758
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