List of variants in gene CTSA reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000308.4(CTSA):c.1088+10C>T	rs4608591	0.65654
NM_000308.4(CTSA):c.948+7G>A	rs2075961	0.65493
NM_000308.4(CTSA):c.33GCT[7] (p.Leu19del)	rs72555383

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