List of variants in gene CPA1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001868.4(CPA1):c.371C>T (p.Thr124Ile)	rs150653308	0.00165
NM_001868.4(CPA1):c.492G>A (p.Thr164=)	rs369058363	0.00016
NM_001868.4(CPA1):c.147+5G>C
NM_001868.4(CPA1):c.788-5C>G	rs201705049

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