chr9:133635393:T>C Detail (hg38) (DBH)

Information

Genome

Assembly Position
hg19 chr9:136,500,515-136,500,515 View the variant detail on this assembly version.
hg38 chr9:133,635,393-133,635,393

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.827
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance not provided
Review star
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
not provided no assertion provided Orthostatic hypotension 1 germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 epilepsy Stage 1 analysis included 290 patients with epilepsy and revealed a higher load ... BeFree 22881836 Detail
<0.001 epilepsy Stage 1 analysis included 290 patients with epilepsy and revealed a higher load ... BeFree 22881836 Detail
0.002 cocaine dependence The influence of dopamine β-hydroxylase gene polymorphism rs1611115 on levodopa/... BeFree 24809448 Detail
0.329 attention deficit hyperactivity disorder Gene-gene interaction analysis revealed significant additive effect of DBH rs110... BeFree 21216270 Detail
0.178 attention deficit hyperactivity disorder Gene-gene interaction analysis revealed significant additive effect of DBH rs110... BeFree 21216270 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000787.3(DBH):c.-979T>C AND Orthostatic hypotension 1 ClinVar Detail
Stage 1 analysis included 290 patients with epilepsy and revealed a higher load of adverse psychotro... DisGeNET Detail
Stage 1 analysis included 290 patients with epilepsy and revealed a higher load of adverse psychotro... DisGeNET Detail
The influence of dopamine β-hydroxylase gene polymorphism rs1611115 on levodopa/carbidopa treatment ... DisGeNET Detail
Gene-gene interaction analysis revealed significant additive effect of DBH rs1108580 and DRD4 rs1800... DisGeNET Detail
Gene-gene interaction analysis revealed significant additive effect of DBH rs1108580 and DRD4 rs1800... DisGeNET Detail
Gene
-
dbSNP
rs1611115 dbSNP
Genome
hg38
Position
chr9:133,635,393-133,635,393
Variant Type
snv
Reference Allele
T
Alternative Allele
C
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))
rs1611115
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.8275
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
13868
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16758
Genome browser