List of variants reported as benign for Hereditary pancreatitis by Illumina Laboratory Services, Illumina

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_007272.3(CTRC):c.514A>G (p.Lys172Glu)	rs34949635	0.02786
NM_007272.3(CTRC):c.*83T>C	rs75456156	0.02717
NM_007272.3(CTRC):c.285C>T (p.Asp95=)	rs41307798	0.02352
NM_007272.3(CTRC):c.156C>T (p.Asn52=)	rs77373944	0.00830
NM_007272.3(CTRC):c.690G>A (p.Glu230=)	rs75971387	0.00820
NM_001379610.1(SPINK1):c.163C>T (p.Pro55Ser)	rs111966833	0.00389
NM_007272.3(CTRC):c.760C>T (p.Arg254Trp)	rs121909293	0.00386
NM_007272.3(CTRC):c.703G>A (p.Val235Ile)	rs140993290	0.00024
NM_007272.3(CTRC):c.747G>A (p.Pro249=)	rs150078209	0.00012
NM_007272.3(CTRC):c.494-13A>G	rs762842599	0.00002
NM_001379610.1(SPINK1):c.*34C>T	rs377333227	0.00001
NM_007272.3(CTRC):c.369C>T (p.Ala123=)	rs749606141	0.00001
NM_007272.3(CTRC):c.68C>T (p.Pro23Leu)	rs533967597	0.00001
NM_007272.3(CTRC):c.180C>A (p.Gly60=)	rs497078
NM_007272.3(CTRC):c.180C>T (p.Gly60=)	rs497078

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