Variants with conflicting interpretations "likely pathogenic" from Database of Curated Mutations (DoCM) and "likely benign" from any submitter

Minimum review status of the submission from Database of Curated Mutations (DoCM):		Collection method of the submission from Database of Curated Mutations (DoCM):
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_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_000455.5(STK11):c.1088C>T (p.Thr363Ile)	rs587778695	0.00004

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