Variant (rsID / SNP)

rs167771

rs167771 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DRD3. Location: chromosome 3, position 113,876,275. Clinical significance in the table: Benign.

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Reference-table entries

DRD3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:113876275
Cytoband: 3q13.31
HGVS: NM_000796.6(DRD3):c.383+2327C>T
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.