Variants with conflicting interpretations "benign" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp and "likely benign" from International Society for Gastrointestinal Hereditary Tumours (InSiGHT)

Minimum review status of the submission from Women's Health and Genetics/Laboratory Corporation of America, LabCorp:		Collection method of the submission from Women's Health and Genetics/Laboratory Corporation of America, LabCorp:
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_000249.4(MLH1):c.589-15C>T	rs55658850	0.00582
NM_000251.3(MSH2):c.1737A>G (p.Lys579=)	rs61756467	0.00138
MSH6:c.3647-51_3647-35del17	rs267607687

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