ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by Center for Human Genetics,University of Leuven

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_000257.4(MYH7):c.1128C>A (p.Asp376Glu) rs2231126
NM_000257.4(MYH7):c.1331A>G (p.Asn444Ser) rs730880159
NM_000257.4(MYH7):c.1351C>G (p.Gln451Glu) rs730880871
NM_000257.4(MYH7):c.2047G>C (p.Val683Leu) rs1566532876
NM_000257.4(MYH7):c.3169G>A (p.Gly1057Ser) rs397516179
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354
NM_000257.4(MYH7):c.3637G>A (p.Val1213Met) rs397516182
NM_000257.4(MYH7):c.4145G>A (p.Arg1382Gln) rs727504325
NM_000257.4(MYH7):c.5287G>A (p.Ala1763Thr) rs727504355
NM_000257.4(MYH7):c.5471A>G (p.Asn1824Ser) rs760218400
NM_000257.4(MYH7):c.976G>C (p.Ala326Pro) rs372731424

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.