ClinVar Miner

List of variants in gene CTSD reported as uncertain significance by Department of Pathology and Laboratory Medicine,Sinai Health System

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: 1

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HGVS	dbSNP
NM_001909.5(CTSD):c.294G>A (p.Thr98=)	rs369373285

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