"CFTR-France"[submitter] AND "LOC111674463"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 818101	NG_016465.4:g.18346T>G	CFTR, LOC111674463	Single nucleotide variant	Cystic fibrosis	GBenign
Select item 818099	NM_000492.3(CFTR):c.-85C>G	LOC111674463, CFTR	Single nucleotide variant	Cystic fibrosis	GBenign
Select item 93148	NM_000492.4(CFTR):c.-8G>C	CFTR, LOC111674463	Single nucleotide variant (5 prime UTR variant)	CFTR-related disorders +4 more	GBenign/Likely benign

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