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Variant (rsID / SNP)

rs6280

DRD3

rs6280 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DRD3. Location: chromosome 3, position 113,890,815. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DRD3Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
3:113890815
Cytoband
3q13.31
HGVS
NM_000796.6(DRD3):c.25G>A (p.Gly9Ser)
Allele change
Missense_G9S

Associated conditions / phenotypes

Essential tremor, susceptibility to|Schizophrenia, susceptibility to|Tremor, hereditary essential, 1

Public references

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