List of variants in gene PRSS50 reported as likely benign by Ambry Genetics

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_013270.5(PRSS50):c.667C>T (p.Arg223Trp)	rs759956225	0.00003
NM_013270.5(PRSS50):c.1108A>G (p.Thr370Ala)
NM_013270.5(PRSS50):c.358G>A (p.Val120Met)
NM_013270.5(PRSS50):c.473G>A (p.Arg158His)

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