Variants with conflicting interpretations "uncertain significance" from Claritas Genomics and "benign" from any submitter

Minimum review status of the submission from Claritas Genomics:		Collection method of the submission from Claritas Genomics:
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: 5

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HGVS	dbSNP	gnomAD frequency
NM_020361.5(CPA6):c.799G>A (p.Gly267Arg)	rs61738009	0.00239
NM_000124.4(ERCC6):c.1996C>T (p.Arg666Cys)	rs61760163	0.00179
NM_000124.4(ERCC6):c.3122A>C (p.Gln1041Pro)	rs139007661	0.00179
NM_001110556.2(FLNA):c.4451A>G (p.Gln1484Arg)	rs200130356	0.00081
NM_000124.4(ERCC6):c.3284C>G (p.Pro1095Arg)	rs4253208

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