ClinVar Miner

Variants with conflicting interpretations "likely benign" from EGL Genetic Diagnostics, Eurofins Clinical Diagnostics and "uncertain significance" from Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute

Minimum review status of the submission from EGL Genetic Diagnostics, Eurofins Clinical Diagnostics: Collection method of the submission from EGL Genetic Diagnostics, Eurofins Clinical Diagnostics:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 4
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HGVS dbSNP
NM_000335.5(SCN5A):c.6007T>C (p.Phe2003Leu) rs41311117
NM_004415.4(DSP):c.4489C>T (p.Arg1497Trp) rs148041814
NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu) rs71534278
NM_170707.4(LMNA):c.1930C>T (p.Arg644Cys) rs142000963

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