ClinVar Miner

List of variants in gene MYH6 studied for Primary familial hypertrophic cardiomyopathy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
Download table as spreadsheet
HGVS dbSNP
NM_002471.3(MYH6):c.1002+3G>A rs869025475
NM_002471.3(MYH6):c.1663G>A (p.Asp555Asn) rs730880149
NM_002471.3(MYH6):c.1702C>T (p.Arg568Cys) rs149650190
NM_002471.3(MYH6):c.1763A>C (p.Asp588Ala) rs142992009
NM_002471.3(MYH6):c.2591C>T (p.Thr864Met) rs200153625
NM_002471.3(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3347G>A (p.Arg1116His) rs369247906
NM_002471.3(MYH6):c.345T>C (p.Tyr115=) rs770221652
NM_002471.3(MYH6):c.3893C>T (p.Ala1298Val) rs368588052
NM_002471.3(MYH6):c.4136C>T (p.Thr1379Met) rs145611185
NM_002471.3(MYH6):c.4144A>G (p.Ile1382Val) rs1555333536
NM_002471.3(MYH6):c.4328C>A (p.Ala1443Asp) rs727503234
NM_002471.3(MYH6):c.4369G>A (p.Glu1457Lys) rs267606905
NM_002471.3(MYH6):c.4595G>T (p.Arg1532Leu) rs34330111
NM_002471.3(MYH6):c.4768C>A (p.Arg1590Ser) rs544624250
NM_002471.3(MYH6):c.4918G>A (p.Glu1640Lys) rs748924413
NM_002471.3(MYH6):c.5257G>C (p.Ala1753Pro) rs142437308
NM_002471.3(MYH6):c.5293G>A (p.Ala1765Thr) rs397516775
NM_002471.3(MYH6):c.5348G>A (p.Arg1783His) rs745473249
NM_002471.3(MYH6):c.5594G>A (p.Arg1865Gln) rs138720701
NM_002471.3(MYH6):c.5780G>T (p.Arg1927Leu) rs730880152
NM_002471.3(MYH6):c.643-5C>T rs199859986
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.