ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Fundacion Favaloro, PRICAI and "uncertain significance" from any submitter

Minimum review status of the submission from Fundacion Favaloro, PRICAI: Collection method of the submission from Fundacion Favaloro, PRICAI:
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.1981C>G (p.Pro661Ala) rs1182317785

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