Varaico: Literature-Extracted Genetic Variants

Gene:MYH6
Variant:p.R17H
Back to variants list

MYH6

NM_002471.4:p.R17H

Associated Papers

Clinically Actionable Hypertrophic Cardiomyopathy Genes in South Asian Indian Patients.

Rao VJ et al.

Journal of the American Heart Association, 2025

41128141 (PubMed )
Supplement: JAH3-14-e042036-s001.pdf

MYH6 in Congenital Heart Defects: A Genotype-Phenotype Characterization in a French Cohort.

Daire E et al.

Pediatric Cardiology, 2025

Significance of α-Myosin Heavy Chain (MYH6) Variants in Hypoplastic Left Heart Syndrome and Related Cardiovascular Diseases.

Anfinson M et al.

Journal of Cardiovascular Development and Disease, 2022

Heavy and light roles: myosin in the morphogenesis of the heart.

England J et al.

Cellular and Molecular Life Sciences : Cmls, 2013

Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects.

Posch MG et al.

Plos One, 2011

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."