Variants with conflicting interpretations "pathogenic" from Database of Curated Mutations (DoCM) and "likely pathogenic" 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005228.5(EGFR):c.2369C>T (p.Thr790Met)	rs121434569	0.00006
NM_000314.8(PTEN):c.389G>A (p.Arg130Gln)	rs121909229
NM_006218.4(PIK3CA):c.1633G>A (p.Glu545Lys)	rs104886003
NM_022552.5(DNMT3A):c.2645G>A (p.Arg882His)	rs147001633

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