Variant (rsID / SNP)

rs1799971

rs1799971 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OPRM1. Location: chromosome 6, position 154,360,797. Clinical significance in the table: Uncertain significance; drug response.

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Reference-table entries

OPRM1Uncertain significance

Clinical significance (as recorded): Uncertain significance; drug response
Variant type: single nucleotide variant
Chromosome / position: 6:154360797
Cytoband: 6q25.2
HGVS: NM_000914.5(OPRM1):c.118A>G (p.Asn40Asp)
Allele change: Silent

Associated conditions / phenotypes

Opioid dependence, susceptibility to, 1|Tramadol response

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.