Variant (rsID / SNP)

rs1042114

rs1042114 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OPRD1. Location: chromosome 1, position 29,138,975. The table records no clinical significance for this variant.

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Reference-table entries

OPRD1Not classified

Variant type: missense_variant
Chromosome / position: 1:29138975
HGVS: NM_000911.4,c.80G>T,p.Cys27Phe
Allele change: Missense_C27F

Associated conditions / phenotypes

Opioid Addiction|Novelty Seeking Personality Trait|Alzheimer Disease

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.