RS113993968 HTRA1

Health Risk Chr 10:122489603
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What This Variant Does
"[OMIM:?]
Associated Conditions
CARASIL syndrome
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 2
CARASIL syndrome
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 2
Other Variants in HTRA1
rs11200638 rs113993971 rs113993970 rs113993969 rs587776873 rs587776445 rs587776446 rs587776448 rs864622781 rs781563777
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