Variant (rsID / SNP)

rs540825

rs540825 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OPRM1. Location: chromosome 6, position 154,414,446. Clinical significance in the table: drug_response.

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Reference-table entries

OPRM1Drug response

Clinical significance (as recorded): drug_response
Variant type: missense_variant
Chromosome / position: 6:154414446
HGVS: NM_001008505.2,c.1206A>T,p.Gln402His
Allele change: Silent

Associated conditions / phenotypes

Mental Depression|Major Depressive Disorder|Depression|Opioid Addiction

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.