ClinVar Miner

List of variants reported as uncertain significance for Hereditary pancreatitis by Mendelics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001379610.1(SPINK1):c.101A>G (p.Asn34Ser)	rs17107315	0.00797
NM_000492.4(CFTR):c.1046C>T (p.Ala349Val)	rs121909021	0.00015
NM_000492.4(CFTR):c.1558G>A (p.Val520Ile)	rs77646904

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