Variants with conflicting interpretations "pathogenic" from Unidad de Genómica Médica UC, Pontificia Universidad Católica de Chile and "likely 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:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_000784.4(CYP27A1):c.1183C>T (p.Arg395Cys)	rs121908096	0.00031
NM_006412.4(AGPAT2):c.493-1G>C	rs606231168	0.00001
NM_000162.5(GCK):c.781G>A (p.Gly261Arg)	rs104894008
NM_000784.4(CYP27A1):c.256-1G>T	rs886556800

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