ClinVar Miner

Variants in gene combination MYH8, MYHAS with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 10
Download table as spreadsheet
NM_002472.3(MYH8):c.1907C>T (p.Ala636Val) rs34693726
NM_002472.3(MYH8):c.2016C>T (p.Phe672=) rs12936716
NM_002472.3(MYH8):c.3117G>A (p.Gly1039=) rs3744553
NM_002472.3(MYH8):c.3270C>T (p.Ile1090=) rs3744552
NM_002472.3(MYH8):c.3686T>C (p.Met1229Thr) rs35962914
NM_002472.3(MYH8):c.4233C>T (p.Asn1411=) rs138992963
NM_002472.3(MYH8):c.5074T>C (p.Trp1692Arg) rs8069834
NM_002472.3(MYH8):c.5208C>T (p.Asp1736=) rs33969260
NM_002472.3(MYH8):c.5350C>G (p.Arg1784Gly) rs141215006
NM_002472.3(MYH8):c.714T>C (p.Thr238=) rs8068729

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.