ClinVar Miner

Variants with conflicting interpretations "benign" from Clinical Genetics, Academic Medical Center and "uncertain significance" from Clinical Genetics, Erasmus University Medical Center

Minimum review status of the submission from Clinical Genetics, Academic Medical Center: Collection method of the submission from Clinical Genetics, Academic Medical Center:
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_014000.3(VCL):c.2388G>A (p.Pro796=) rs767809 0.42862

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