C0010674[trait identifier] AND "Institute of Human Genetics, Cologne U - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 560220	NM_000492.4(CFTR):c.1329_1350del (p.Asp443fs)	CFTR-AS1, CFTR (D443fs)	Deletion (frameshift variant)	Cystic fibrosis	GLikely pathogenic
Select item 982045	NM_000492.4(CFTR):c.2909-1G>C	CFTR	Single nucleotide variant (splice acceptor variant)	Cystic fibrosis	GPathogenic