RS781563777 HTRA1

Health Risk Chr 10:122488946
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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
Other Variants in HTRA1
rs11200638 rs113993971 rs113993970 rs113993969 rs113993968 rs587776873 rs587776445 rs587776446 rs587776448 rs864622781
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