Variant (rsID / SNP)

rs4532

rs4532 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DRD1. Location: chromosome 5, position 174,870,150. Clinical significance in the table: Benign.

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Reference-table entries

DRD1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:174870150
Cytoband: 5q35.2
HGVS: NM_000794.5(DRD1):c.-48=
Allele change: Silent

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.