Variants with conflicting interpretations "uncertain significance" from ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories and "likely pathogenic" from Mayo Clinic Laboratories, Mayo Clinic

Minimum review status of the submission from ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories:		Collection method of the submission from ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_018706.7(DHTKD1):c.2185G>A (p.Gly729Arg)	rs117225135	0.00190
NM_000463.3(UGT1A1):c.674T>G (p.Val225Gly)	rs35003977	0.00034
NM_024301.5(FKRP):c.898G>A (p.Val300Met)	rs563033008	0.00031
NM_003060.4(SLC22A5):c.761G>A (p.Arg254Gln)	rs200699819	0.00007
NM_000431.4(MVK):c.1139A>G (p.His380Arg)	rs104895324	0.00005
NM_000492.4(CFTR):c.3083T>G (p.Met1028Arg)	rs397508494	0.00001
NM_000138.5(FBN1):c.7540G>A (p.Gly2514Arg)	rs363811

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