List of variants in gene MYOM1 reported as benign for Cardiovascular phenotype

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003803.4(MYOM1):c.3576-5C>T	rs7232329	0.36941
NM_003803.4(MYOM1):c.4662C>T (p.Ala1554=)	rs1143657	0.18160
NM_003803.4(MYOM1):c.66G>C (p.Val22=)	rs1662316	0.10760
NM_003803.4(MYOM1):c.644C>T (p.Thr215Met)	rs2230165	0.07696
NM_003803.4(MYOM1):c.4222G>A (p.Asp1408Asn)	rs3765623	0.05400
NM_003803.4(MYOM1):c.4358T>C (p.Met1453Thr)	rs16944397	0.05084
NM_003803.4(MYOM1):c.1799A>T (p.Glu600Val)	rs9807556	0.01756
NM_003803.4(MYOM1):c.2673G>C (p.Leu891=)	rs115240600	0.01425
NM_003803.4(MYOM1):c.2210-4T>G	rs143030509	0.01023
NM_003803.4(MYOM1):c.4718G>A (p.Arg1573Gln)	rs117342470	0.00758
NM_003803.4(MYOM1):c.139A>G (p.Ser47Gly)	rs202145133	0.00695
NM_003803.4(MYOM1):c.2110G>A (p.Glu704Lys)	rs149528866	0.00679
NM_003803.4(MYOM1):c.539C>T (p.Thr180Ile)	rs61735396	0.00612
NM_003803.4(MYOM1):c.1900+3A>C	rs77613865	0.00536
NM_003803.4(MYOM1):c.2179A>G (p.Thr727Ala)	rs115382168	0.00345
NM_003803.4(MYOM1):c.64G>C (p.Val22Leu)	rs1791085

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.