ClinVar Miner

List of variants in gene combination CFTR, LOC111674477 reported as likely benign for Hereditary pancreatitis

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000492.4(CFTR):c.4243-5C>T	rs114402068	0.00138
NM_000492.4(CFTR):c.4243-20A>G	rs138025486	0.00086

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