ClinVar Miner

List of variants in gene CST3 studied for Hereditary cerebral amyloid angiopathy, Icelandic type

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000099.4(CST3):c.281T>A (p.Leu94Gln)	rs28939068
NM_000099.4(CST3):c.340C>T (p.Gln114Ter)	rs1600363764
NM_000099.4(CST3):c.376C>T (p.Gln126Ter)	rs2515343230

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