List of variants in gene combination PRSS48, SH3D19 reported as likely benign

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_183375.5(PRSS48):c.343G>A (p.Val115Ile)	rs192149727	0.00009
NM_183375.5(PRSS48):c.533G>A (p.Arg178His)	rs372546589	0.00005
NM_183375.5(PRSS48):c.79C>T (p.Arg27Cys)	rs776335390	0.00002
NM_183375.5(PRSS48):c.26C>T (p.Thr9Met)
NM_183375.5(PRSS48):c.82G>A (p.Val28Ile)
NM_183375.5(PRSS48):c.837C>A (p.Phe279Leu)

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