Variants with conflicting interpretations "likely pathogenic" from Watson Genetic Lab and "pathogenic" from any submitter

Minimum review status of the submission from Watson Genetic Lab:		Collection method of the submission from Watson Genetic Lab:
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_000175.5(GPI):c.1574T>C (p.Ile525Thr)	rs137853584	0.00001
NM_014975.3(MAST1):c.580GAG[1] (p.Glu195del)	rs1568408280

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