OPRM1 c.290+11468C>T

Variant ID: 6-154372437-C-T

NM_000914.3(OPRM1):c.290+11468C>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs607759
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs607759
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal
Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV
Publication Date: 2012-12

Variant appearance in text: rs607759
PubMed Link: 21808284
Variant Present in the following documents:
  • NIHMS305090-supplement-3.pdf
View BVdb publication page



Haplotype block structure of the genomic region of the mu opioid receptor gene.

Journal Of Human Genetics
Levran, Orna O; Awolesi, Olaoluwakitan O; Linzy, Shirley S; Adelson, Miriam M; Kreek, Mary Jeanne MJ
Publication Date: 2011-02

Variant appearance in text: rs607759
PubMed Link: 21160491
Variant Present in the following documents:
  • Main text
  • nihms-252057.pdf
View BVdb publication page



Evaluation of a SNP map of 6q24-27 confirms diabetic nephropathy loci and identifies novel associations in type 2 diabetes patients with nephropathy from an African-American population.

Human Genetics
Leak, Tennille S TS; Mychaleckyj, Josyf C JC; Smith, Shelly G SG; Keene, Keith L KL; Gordon, Candace J CJ; Hicks, Pamela J PJ; Freedman, Barry I BI; Bowden, Donald W DW; Sale, Michèle M MM
Publication Date: 2008-08

Variant appearance in text: rs607759
PubMed Link: 18560894
Variant Present in the following documents:
  • Main text
View BVdb publication page



Clone-based systematic haplotyping (CSH): a procedure for physical haplotyping of whole genomes.

Genome Research
Burgtorf, Carola C; Kepper, Pamela P; Hoehe, Margret M; Schmitt, Carsten C; Reinhardt, Richard R; Lehrach, Hans H; Sauer, Sascha S
Publication Date: 2003-12

Variant appearance in text: rs607759
PubMed Link: 14656974
Variant Present in the following documents:
  • Main text
View BVdb publication page



MALDI mass spectrometry analysis of single nucleotide polymorphisms by photocleavage and charge-tagging.

Nucleic Acids Research
Sauer, Sascha S; Lehrach, Hans H; Reinhardt, Richard R
Publication Date: 2003-06-01

Variant appearance in text: rs607759
PubMed Link: 12771227
Variant Present in the following documents:
  • Main text
View BVdb publication page