ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Unidad de Genómica Médica UC, Pontificia Universidad Católica de Chile and "pathogenic" from any submitter

Minimum review status of the submission from Unidad de Genómica Médica UC, Pontificia Universidad Católica de Chile: Collection method of the submission from Unidad de Genómica Médica UC, Pontificia Universidad Católica de Chile:
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_000784.4(CYP27A1):c.1185-1G>T rs587778779

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