Variants with conflicting interpretations "benign" from Counsyl and "pathogenic" from any submitter

Minimum review status of the submission from Counsyl:		Collection method of the submission from Counsyl:
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_000155.4(GALT):c.940A>G (p.Asn314Asp)	rs2070074	0.07384
NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr)	rs33935154	0.01316
NM_007294.4(BRCA1):c.4327C>G (p.Arg1443Gly)	rs41293455

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