List of variants reported as likely benign for Hereditary pancreatitis by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 35

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HGVS	dbSNP	gnomAD frequency
NM_002769.5(PRSS1):c.567T>C (p.Leu189=)	rs377124851	0.00444
NM_007272.3(CTRC):c.555G>A (p.Thr185=)	rs113087202	0.00097
NM_007272.3(CTRC):c.494-6C>T	rs111790169	0.00096
NM_007272.3(CTRC):c.40+24G>A	rs142888713	0.00071
NM_007272.3(CTRC):c.640-14C>T	rs202049497	0.00060
NM_007272.3(CTRC):c.231-14C>T	rs374364850	0.00046
NM_007272.3(CTRC):c.110G>A (p.Arg37Gln)	rs145868278	0.00032
NM_007272.3(CTRC):c.27G>A (p.Ala9=)	rs374821228	0.00016
NM_007272.3(CTRC):c.747G>A (p.Pro249=)	rs150078209	0.00012
NM_007272.3(CTRC):c.356+17C>G	rs376786664	0.00007
NM_002769.5(PRSS1):c.591+8G>C	rs371601976	0.00006
NM_007272.3(CTRC):c.678C>T (p.Asn226=)	rs777608312	0.00006
NM_007272.3(CTRC):c.493+3G>A	rs772436044	0.00004
NM_007272.3(CTRC):c.356+7G>C	rs773334021	0.00003
NM_007272.3(CTRC):c.494-13A>G	rs762842599	0.00002
NM_002769.5(PRSS1):c.200+8T>C	rs886038518	0.00001
NM_002769.5(PRSS1):c.81C>T (p.Gly27=)	rs1403836546	0.00001
NM_002769.5(PRSS1):c.93G>A (p.Glu31=)	rs745623963	0.00001
NM_007272.3(CTRC):c.230+7G>A	rs754126755	0.00001
NM_007272.3(CTRC):c.40+18G>A	rs1708076823	0.00001
NM_007272.3(CTRC):c.493+38G>A	rs1488630264	0.00001
NM_007272.3(CTRC):c.639+45A>G	rs776164776	0.00001
NM_002769.5(PRSS1):c.162C>T (p.Asn54=)	rs148440491
NM_002769.5(PRSS1):c.201C>A (p.Ser67=)
NM_002769.5(PRSS1):c.592-8C>A	rs200381474
NM_007272.3(CTRC):c.147C>T (p.Tyr49=)
NM_007272.3(CTRC):c.249T>C (p.Arg83=)	rs1570783555
NM_007272.3(CTRC):c.357-3C>T
NM_007272.3(CTRC):c.363T>C (p.Asp121=)
NM_007272.3(CTRC):c.45C>T (p.Ser15=)
NM_007272.3(CTRC):c.640-40G>C	rs191025876
NM_007272.3(CTRC):c.640-40G>T	rs191025876
NM_007272.3(CTRC):c.640-41G>T	rs186735838
NM_007272.3(CTRC):c.640-42G>C	rs199897030
NM_007272.3(CTRC):c.747G>T (p.Pro249=)	rs150078209

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