Variant (rsID / SNP)

rs2229205

rs2229205 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OPRL1. Location: chromosome 20, position 62,729,431. The table records no clinical significance for this variant.

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Reference-table entries

OPRL1Not classified

Variant type: synonymous_variant
Chromosome / position: 20:62729431
HGVS: NM_001318853.2,c.510C>T,p.Val170Val
Allele change: Synonymous_V170V

Associated conditions / phenotypes

Smoking As a Quantitative Trait Locus 3|Tobacco 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.