OPRM1 A118G associated_with OPRM1

Separate analyses conditioning on rs1799971 ... to assess the interdependence of OPRM1 signals.

The variant identified is the long‑studied rs1799971 (OPRM1‑A118G), a functional coding variant ... in the mu opioid receptor gene (OPRM1).

major functional OPRM1 SNP

Asp40 carriers of the OPRM1 gene ...

The most frequently studied polymorphism is the Asn40Asp SNP of the OPRM1 gene.

The A118G single nucleotide polymorphism (SNP) of the human µ opioid receptor gene (OPRM1)...

The small number of pharmacogenetic studies analyzing the role of OPRM1 in nicotine dependence treatment have focused on the A118G polymorphism.

first exon of the human MOPR gene with A118 and G118

The A118G SNP in the OPRM1 gene was assayed using a commercially available instrument and TaqMan assays.

The most studied OPRM1 variant is the non-synonymous variant rs1799971 (118A>G, Asn40Asp).

A118G SNP of the OPRM1 gene

participants were prospectively genotyped at the A118G variant of OPRM1.

As the 118A>G SNP changes an amino acid, it has been generally assumed that it is the causative variant for the phenotypes associated with it.

in addition to the A118G SNP of the OPRM1

prospective genotyping based on the A118G SNP of the OPRM1 gene

a common functional missense variant of the μ-opioid receptor (OPRM1 Asn40Asp)

individuals carrying one or two copies of the variant 118G allele (118AG or 118GG genotype ...) of the OPRM1 polymorphism

The non-synonymous variant rs1799971 (118A>G, Asn40Asp) ...

The most frequently studied OPRM1 variant is the single nucleotide polymorphism (SNP) A118G ... in exon 1