Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000222752 | SCV000271903 | uncertain significance | not specified | 2018-05-02 | criteria provided, single submitter | clinical testing | The p.Gln408Glu variant in LAMP2 has not been previously reported in individuals with cardiomyopathy or in large population studies. Computational prediction to ols and conservation analysis suggest that this variant may not impact the prote in but these data are insufficient to rule out a role in disease. In summary, th e clinical significance of the p.Gln408Glu variant is uncertain. ACMG/AMP Criter ia applied: PM2; BP4. |