List of variants in gene combination PRSS1, TRB reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002769.5(PRSS1):c.508A>G (p.Lys170Glu)	rs201550522	0.00006
NM_002769.5(PRSS1):c.674A>G (p.Lys225Arg)	rs541223359	0.00006
NM_002769.5(PRSS1):c.240C>T (p.Val80=)	rs772622287	0.00002
NM_002769.5(PRSS1):c.93G>A (p.Glu31=)	rs745623963	0.00001
NM_002769.5(PRSS1):c.162C>T (p.Asn54=)	rs148440491
NM_002769.5(PRSS1):c.328T>C (p.Leu110=)
NM_002769.5(PRSS1):c.330A>G (p.Leu110=)
NM_002769.5(PRSS1):c.360C>T (p.Asn120=)	rs606231348
NM_002769.5(PRSS1):c.468C>T (p.Asp156=)	rs146076691
NM_002769.5(PRSS1):c.510G>A (p.Lys170=)	rs750427023

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.