Variants with conflicting interpretations "benign" from Counsyl and "likely 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_001692.4(ATP6V1B1):c.481G>A (p.Glu161Lys)	rs114234874	0.02502
NM_014363.6(SACS):c.13717A>C (p.Asn4573His)	rs34382952	0.00326

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