ClinVar Miner

List of variants in gene MYH6 reported as uncertain significance by Blueprint Genetics,

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
NM_002471.3(MYH6):c.1002+3G>A rs869025475
NM_002471.3(MYH6):c.1048G>A (p.Val350Ile) rs200260629
NM_002471.3(MYH6):c.1171C>A (p.Leu391Met) rs869025472
NM_002471.3(MYH6):c.1663G>A (p.Asp555Asn) rs730880149
NM_002471.3(MYH6):c.2538G>C (p.Glu846Asp) rs730880150
NM_002471.3(MYH6):c.2575G>T (p.Gly859Trp) rs369274077
NM_002471.3(MYH6):c.2591C>T (p.Thr864Met) rs200153625
NM_002471.3(MYH6):c.2612G>A (p.Arg871His) rs869025473
NM_002471.3(MYH6):c.3105+9T>C rs1555333942
NM_002471.3(MYH6):c.3133A>G (p.Lys1045Glu) rs869025474
NM_002471.3(MYH6):c.4136C>T (p.Thr1379Met) rs145611185
NM_002471.3(MYH6):c.4216G>A (p.Val1406Met) rs201566738
NM_002471.3(MYH6):c.4328C>A (p.Ala1443Asp) rs727503234
NM_002471.3(MYH6):c.4713G>T (p.Lys1571Asn) rs730880151
NM_002471.3(MYH6):c.4918G>A (p.Glu1640Lys) rs748924413
NM_002471.3(MYH6):c.5336C>A (p.Ala1779Asp) rs769271404
NM_002471.3(MYH6):c.5780G>T (p.Arg1927Leu) rs730880152
NM_002471.3(MYH6):c.5796G>A (p.Lys1932=) rs730880153
NM_002471.3(MYH6):c.694G>A (p.Gly232Ser) rs587782960

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.