List of variants in gene combination PRSS1, TRB reported as benign for not specified

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: 19

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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.567T>C (p.Leu189=)	rs377124851	0.00444
NM_002769.5(PRSS1):c.592-24C>T	rs192452846	0.00354
NM_002769.5(PRSS1):c.592-11C>T	rs183791770	0.00131
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.292C>A (p.Gln98Lys)	rs750348889	0.00002
NM_002769.4(PRSS1):c.-30_-28delTCC	rs386134264
NM_002769.5(PRSS1):c.146G>T (p.Gly49Val)	rs138464021
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.49C>T (p.Pro17Ser)	rs770782578
NM_002769.5(PRSS1):c.542G>A (p.Ser181Asn)	rs201719096
NM_002769.5(PRSS1):c.637G>A (p.Val213Ile)	rs200902389
NM_002769.5(PRSS1):c.72C>T (p.Ile24=)	rs372637371

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