ClinVar Miner

List of variants in gene MYH6 reported as likely benign by Integrated Genetics/Laboratory Corporation of America

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_002471.3(MYH6):c.1753G>A (p.Gly585Ser) rs150415679
NM_002471.3(MYH6):c.1763A>C (p.Asp588Ala) rs142992009
NM_002471.3(MYH6):c.2890G>T (p.Ala964Ser) rs144907522
NM_002471.3(MYH6):c.3199A>G (p.Ser1067Gly) rs145508517
NM_002471.3(MYH6):c.3979-8_3979-7delinsGC rs727503235
NM_002471.3(MYH6):c.3979-8del rs193922652
NM_002471.3(MYH6):c.4401T>G (p.Ser1467=) rs150081280
NM_002471.3(MYH6):c.5508A>G (p.Ala1836=) rs193922654
NM_002471.3(MYH6):c.5642A>G (p.Lys1881Arg) rs750886219
NM_002471.3(MYH6):c.831G>T (p.Gln277His) rs140660481

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.