Variants with conflicting interpretations "uncertain significance" from Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine and "pathogenic" from any submitter

Minimum review status of the submission from Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine:		Collection method of the submission from Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001218.5(CA12):c.908-1G>A	rs148438059	0.00043
NM_057176.3(BSND):c.35T>C (p.Ile12Thr)	rs121908144	0.00002

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