Variants in gene CFTR with conflicting interpretations "likely pathogenic" and "benign"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP
NM_000492.3(CFTR):c.2506G>T (p.Asp836Tyr)	rs201386642
NM_000492.3(CFTR):c.3485G>T (p.Arg1162Leu)	rs1800120
NM_000492.3(CFTR):c.958T>G (p.Leu320Val)	rs144476686
NM_000492.4(CFTR):c.1865G>A (p.Gly622Asp)	rs121908759
NM_000492.4(CFTR):c.220C>T (p.Arg74Trp)	rs115545701
NM_000492.4(CFTR):c.3808G>A (p.Asp1270Asn)	rs11971167

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