Variants with conflicting interpretations "pathogenic" from Institute of Human Genetics, Heidelberg University and "likely pathogenic" from Baylor Genetics

Minimum review status of the submission from Institute of Human Genetics, Heidelberg University:		Collection method of the submission from Institute of Human Genetics, Heidelberg University:
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_007194.4(CHEK2):c.1427C>T (p.Thr476Met)	rs142763740	0.00032
NM_000346.4(SOX9):c.508C>G (p.Pro170Ala)	rs866706988

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