chr11:113414814:C>A Detail (hg38) (DRD2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:113,285,536-113,285,536 View the variant detail on this assembly version. |
hg38 | chr11:113,414,814-113,414,814 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_016574.3:c.723+607G>T | |
NM_000795.3:c.724-353G>T | ||
Ensemble | ENST00000346454.7:c.723+607G>T |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.383 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2024-01-15 | criteria provided, single submitter | Dystonic disorder |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.010 | Mental Depression | Findings for DAT1 intron8 were also significant for two EMD subscales, generaliz... | BeFree | 24780147 | Detail |
0.024 | Mental Depression | Findings for DAT1 intron8 were also significant for two EMD subscales, generaliz... | BeFree | 24780147 | Detail |
0.155 | attention deficit hyperactivity disorder | DRD2 rs2283265 was associated with teachers' global ratings of ADHD (ηp(2)=.052)... | BeFree | 24780147 | Detail |
<0.001 | anxiety generalized | DAT1 intron8 was associated with parent-rated hyperactivity (ηp(2)=.045) and bot... | BeFree | 24780147 | Detail |
0.340 | attention deficit hyperactivity disorder | Three dopamine transporter gene (SLC6A3/DAT1) polymorphisms (intron8 5/6 VNTR, 3... | BeFree | 24780147 | Detail |
0.002 | Inattention | DAT1 intron8 was associated with parent-rated hyperactivity (ηp(2)=.045) and bot... | BeFree | 24780147 | Detail |
0.002 | depressive disorder | Findings for DAT1 intron8 were also significant for two EMD subscales, generaliz... | BeFree | 24780147 | Detail |
0.345 | schizophrenia | We assessed catechol-O-methyltransferase (COMT) Val108/158Met (rs4680) and dopam... | BeFree | 24495967 | Detail |
0.291 | schizophrenia | We assessed catechol-O-methyltransferase (COMT) Val108/158Met (rs4680) and dopam... | BeFree | 24495967 | Detail |
0.082 | depressive disorder | Findings for DAT1 intron8 were also significant for two EMD subscales, generaliz... | BeFree | 24780147 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000795.4(DRD2):c.724-353G>T AND Dystonic disorder | ClinVar | Detail |
Findings for DAT1 intron8 were also significant for two EMD subscales, generalized anxiety (ηp(2)=.0... | DisGeNET | Detail |
Findings for DAT1 intron8 were also significant for two EMD subscales, generalized anxiety (ηp(2)=.0... | DisGeNET | Detail |
DRD2 rs2283265 was associated with teachers' global ratings of ADHD (ηp(2)=.052). | DisGeNET | Detail |
DAT1 intron8 was associated with parent-rated hyperactivity (ηp(2)=.045) and both DAT1 9/10 VNTR (ηp... | DisGeNET | Detail |
Three dopamine transporter gene (SLC6A3/DAT1) polymorphisms (intron8 5/6 VNTR, 3'-UTR 9/10 VNTR, rs2... | DisGeNET | Detail |
DAT1 intron8 was associated with parent-rated hyperactivity (ηp(2)=.045) and both DAT1 9/10 VNTR (ηp... | DisGeNET | Detail |
Findings for DAT1 intron8 were also significant for two EMD subscales, generalized anxiety (ηp(2)=.0... | DisGeNET | Detail |
We assessed catechol-O-methyltransferase (COMT) Val108/158Met (rs4680) and dopamine D2 receptor (DRD... | DisGeNET | Detail |
We assessed catechol-O-methyltransferase (COMT) Val108/158Met (rs4680) and dopamine D2 receptor (DRD... | DisGeNET | Detail |
Findings for DAT1 intron8 were also significant for two EMD subscales, generalized anxiety (ηp(2)=.0... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs2283265 dbSNP
- Genome
- hg38
- Position
- chr11:113,414,814-113,414,814
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- A
- 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))
- rs2283265
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.3827
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 6413
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16758
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