List of variants in gene combination MYH8, MYHAS reported as likely benign for MYH8-related disorder

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002472.3(MYH8):c.143C>T (p.Ser48Phe)	rs146669648	0.00101
NM_002472.3(MYH8):c.4042G>A (p.Glu1348Lys)	rs140562514	0.00083
NM_002472.3(MYH8):c.954G>C (p.Gln318His)	rs142606252	0.00081
NM_002472.3(MYH8):c.430G>C (p.Ala144Pro)	rs138262102	0.00065
NM_002472.3(MYH8):c.4878T>C (p.Asn1626=)	rs202123184	0.00055
NM_002472.3(MYH8):c.4147A>G (p.Ile1383Val)	rs138607111	0.00045
NM_002472.3(MYH8):c.304C>G (p.Pro102Ala)	rs149941951	0.00014
NM_002472.3(MYH8):c.4353C>T (p.Asn1451=)	rs756865778	0.00007
NM_002472.3(MYH8):c.417C>T (p.Pro139=)	rs531526832	0.00005
NM_002472.3(MYH8):c.355-9T>C	rs776667568	0.00001
NM_002472.3(MYH8):c.4962+7G>A	rs770966811	0.00001
NM_002472.3(MYH8):c.105T>C (p.Asp35=)
NM_002472.3(MYH8):c.405G>T (p.Pro135=)	rs775704195

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.