RS864622781 HTRA1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 2
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 2
CARASIL syndrome
Cerebral arterial disease
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 2
Cerebral arteriopathy
Other Variants in HTRA1