Variants with conflicting interpretations "pathogenic" from Institute of Medical and Molecular Genetics, Hospital Universitario La Paz and "likely pathogenic" from any submitter

Minimum review status of the submission from Institute of Medical and Molecular Genetics, Hospital Universitario La Paz:		Collection method of the submission from Institute of Medical and Molecular Genetics, Hospital Universitario La Paz:
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_002067.5(GNA11):c.547C>T (p.Arg183Cys)	rs1555702147
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg)	rs121913272
NM_006218.4(PIK3CA):c.1633G>A (p.Glu545Lys)	rs104886003
NM_006218.4(PIK3CA):c.3140A>G (p.His1047Arg)	rs121913279

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