Variants with conflicting interpretations "likely pathogenic" from Familial Cancer Clinic, Veneto Institute of Oncology and "pathogenic" from any submitter

Minimum review status of the submission from Familial Cancer Clinic, Veneto Institute of Oncology:		Collection method of the submission from Familial Cancer Clinic, Veneto Institute of Oncology:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_017849.4(TMEM127):c.117_120del (p.Ile41fs)	rs121908816
NM_017849.4(TMEM127):c.265_268del (p.Thr89fs)	rs121908822
NM_017849.4(TMEM127):c.410-2A>C	rs121908826

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