Variant (rsID / SNP)

rs1800499

rs1800499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DRD2. Location: chromosome 11, position 113,287,694. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DRD2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:113287694
Cytoband: 11q23.2
HGVS: NM_000795.4(DRD2):c.423G>A (p.Leu141=)
Allele change: Synonymous_L141L

Associated conditions / phenotypes

Dystonic disorder

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.