Variants with conflicting interpretations "uncertain significance" from Molecular Genetics Lab, CHRU Brest and "likely benign" from any submitter

Minimum review status of the submission from Molecular Genetics Lab, CHRU Brest:		Collection method of the submission from Molecular Genetics Lab, CHRU Brest:
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_182760.4(SUMF1):c.664G>C (p.Gly222Arg)	rs137917233	0.00180
NM_001291303.3(FAT4):c.11260A>G (p.Ser3754Gly)	rs79909102	0.00061

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