ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Cardiovascular Biomarker Research Laboratory, Mayo Clinic and "likely pathogenic" from Molecular Genetics Laboratory, Centre for Cardiovascular Surgery and Transplantation

Minimum review status of the submission from Cardiovascular Biomarker Research Laboratory, Mayo Clinic: Collection method of the submission from Cardiovascular Biomarker Research Laboratory, Mayo Clinic:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_000527.5(LDLR):c.1238C>T (p.Thr413Met) rs368562025 0.00001

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