ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Medical Genetics UMG, Mater Domini University Hospital/ Magna Graecia University of Catanzaro and "likely pathogenic" from any submitter

Minimum review status of the submission from Medical Genetics UMG, Mater Domini University Hospital/ Magna Graecia University of Catanzaro: Collection method of the submission from Medical Genetics UMG, Mater Domini University Hospital/ Magna Graecia University of Catanzaro:
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_007294.4(BRCA1):c.134+2T>G rs80358131

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