ADH1C c.567+62G>A

Variant ID: 4-100265957-C-T

NM_000669.3(ADH1C):c.567+62G>A

This variant was identified in 4 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: rs283411
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: rs283411
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Cerebrospinal fluid APOE levels: an endophenotype for genetic studies for Alzheimer's disease.

Human Molecular Genetics
Cruchaga, Carlos C; Kauwe, John S K JS; Nowotny, Petra P; Bales, Kelly K; Pickering, Eve H EH; Mayo, Kevin K; Bertelsen, Sarah S; Hinrichs, Anthony A; , ; Fagan, Anne M AM; Holtzman, David M DM; Morris, John C JC; Goate, Alison M AM
Publication Date: 2012-10-15

Variant appearance in text: rs283411
PubMed Link: 22821396
Variant Present in the following documents:
  • Main text
View BVdb publication page



ADH single nucleotide polymorphism associations with alcohol metabolism in vivo.

Human Molecular Genetics
Birley, Andrew J AJ; James, Michael R MR; Dickson, Peter A PA; Montgomery, Grant W GW; Heath, Andrew C AC; Martin, Nicholas G NG; Whitfield, John B JB
Publication Date: 2009-04-15

Variant appearance in text: rs283411
PubMed Link: 19193628
Variant Present in the following documents:
  • Main text
View BVdb publication page