Variants with conflicting interpretations "benign" from St. Jude Molecular Pathology, St. Jude Children's Research Hospital and "benign" from International Society for Gastrointestinal Hereditary Tumours (InSiGHT)

Minimum review status of the submission from St. Jude Molecular Pathology, St. Jude Children's Research Hospital:		Collection method of the submission from St. Jude Molecular Pathology, St. Jude Children's Research Hospital:
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_000249.4(MLH1):c.1852_1853delinsGC (p.Lys618Ala)	rs35502531

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