ClinVar Miner

List of variants reported as pathogenic for Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 by OMIM

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Total variants: 4

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HGVS	dbSNP
NM_002775.5(HTRA1):c.497G>T (p.Arg166Leu)	rs864622781
NM_002775.5(HTRA1):c.517G>C (p.Ala173Pro)	rs781563777
NM_002775.5(HTRA1):c.852C>A (p.Ser284Arg)	rs864622782
NM_002775.5(HTRA1):c.973-1G>A	rs864622783

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