Variants with conflicting interpretations "likely pathogenic" from Center for Individualized Medicine, Mayo Clinic and "pathogenic" from Invitae

Minimum review status of the submission from Center for Individualized Medicine, Mayo Clinic:		Collection method of the submission from Center for Individualized Medicine, Mayo Clinic:
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_000135.4(FANCA):c.4015del (p.Leu1339fs)	rs762902309	0.00004
NM_000051.4(ATM):c.4111del	rs797045114
NM_000553.6(WRN):c.487_488del (p.Asp163fs)	rs797045118

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