List of variants in gene CTSD reported as likely pathogenic for dementia

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001909.5(CTSD):c.299C>T (p.Ser100Phe)	rs796052407	0.00004
NM_001909.5(CTSD):c.675_704+1dup
NM_001909.5(CTSD):c.68+1G>A
NM_001909.5(CTSD):c.683TCT[1] (p.Phe229del)	rs1057519591
NM_001909.5(CTSD):c.704+1G>T
NM_001909.5(CTSD):c.824_827+30del	rs2133659840
NM_001909.5(CTSD):c.827+2T>C	rs1845791308
NM_001909.5(CTSD):c.828-2A>C
NM_001909.5(CTSD):c.972+1G>C

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