List of variants in gene HTRA1 reported as uncertain significance for CARASIL syndrome

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002775.5(HTRA1):c.1333G>A (p.Ala445Thr)	rs371279115	0.00013
NM_002775.5(HTRA1):c.589C>T (p.Arg197Ter)	rs1438223502	0.00001
NM_002775.5(HTRA1):c.599C>T (p.Pro200Leu)	rs773396186	0.00001
NM_002775.5(HTRA1):c.854C>T (p.Pro285Leu)	rs587776446

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