List of variants in gene MYH7 reported by Department of Pathology and Laboratory Medicine, Sinai Health System

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.189C>T (p.Thr63=)	rs2069540	0.51584
NM_000257.4(MYH7):c.2967T>C (p.Ile989=)	rs7157716	0.43030
NM_000257.4(MYH7):c.732C>T (p.Phe244=)	rs2069542	0.27385
NM_000257.4(MYH7):c.1062C>T (p.Gly354=)	rs735712	0.06133
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu)	rs45496496	0.00050
NM_000257.4(MYH7):c.3286G>T (p.Asp1096Tyr)	rs45478699	0.00013
NM_000257.4(MYH7):c.3865C>T (p.Arg1289Trp)	rs180824037	0.00001
NM_000257.4(MYH7):c.3337-4dup	rs45504498

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.