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

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

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002769.5(PRSS1):c.738T>C (p.Asn246=)	rs6667	0.53816
NM_002769.5(PRSS1):c.738= (p.Asn246=)	rs6667	0.46184
NM_002769.5(PRSS1):c.567T>C (p.Leu189=)	rs377124851	0.00444
NM_002769.5(PRSS1):c.121C>T (p.Leu41=)	rs369646357	0.00034
NM_002769.5(PRSS1):c.417C>T (p.Cys139=)	rs141847266	0.00032
NM_002769.5(PRSS1):c.40+13C>T	rs368872847	0.00016
NM_002769.5(PRSS1):c.390C>T (p.Thr130=)	rs561097415	0.00012
NM_002769.5(PRSS1):c.366C>T (p.Arg122=)	rs201487096	0.00005
NM_002769.4(PRSS1):c.-30_-28delTCC	rs386134264
NM_002769.5(PRSS1):c.200+17C>T	rs200688125
NM_002769.5(PRSS1):c.200+1G>A	rs143909348
NM_002769.5(PRSS1):c.40+40del	rs748794481
NM_002769.5(PRSS1):c.41-45del
NM_002769.5(PRSS1):c.454+16A>T	rs377570765
NM_002769.5(PRSS1):c.486T>C (p.Asp162=)	rs6666
NM_002769.5(PRSS1):c.72C>T (p.Ile24=)	rs372637371

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