List of variants in gene HTRA1 reported as uncertain significance for Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_002775.5(HTRA1):c.590G>A (p.Arg197Gln)	rs1180835237	0.00001
NM_002775.5(HTRA1):c.835G>A (p.Val279Met)	rs745305935	0.00001
NM_002775.5(HTRA1):c.1127C>T (p.Ala376Val)
NM_002775.5(HTRA1):c.138C>A (p.Cys46Ter)	rs1394472516
NM_002775.5(HTRA1):c.260T>G (p.Leu87Arg)
NM_002775.5(HTRA1):c.283G>T (p.Val95Leu)	rs2133905276
NM_002775.5(HTRA1):c.660C>G (p.His220Gln)	rs1357930157
NM_002775.5(HTRA1):c.857T>C (p.Phe286Ser)
NM_002775.5(HTRA1):c.910G>C (p.Gly304Arg)
NM_002775.5(HTRA1):c.983C>T (p.Ser328Leu)	rs2133449911

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