Variants with conflicting interpretations "pathogenic" from Breast Center, Key Laboratory of Carcinogenesis and Translational Research and "uncertain significance" from any submitter

Minimum review status of the submission from Breast Center, Key Laboratory of Carcinogenesis and Translational Research:		Collection method of the submission from Breast Center, Key Laboratory of Carcinogenesis and Translational Research:
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: 1

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.5522G>A (p.Ser1841Asn)	rs80357368

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