Variant (rsID / SNP)

rs1611115

rs1611115 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DBH. Location: chromosome 9, position 136,500,515. Clinical significance in the table: association.

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Reference-table entries

DBHAssociation

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 9:136500515
Cytoband: 9q34.2
HGVS: NM_000787.3(DBH):c.-979T=

Associated conditions / phenotypes

Dopamine beta-hydroxylase polymorphism

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.