RS1060503242 ACVRL1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Telangiectasia
hereditary hemorrhagic
type 2
Cardiovascular phenotype
ACVRL1-related disorder
Telangiectasia
hereditary hemorrhagic
type 2
Telangiectasia
hereditary hemorrhagic
type 2
Cardiovascular phenotype
ACVRL1-related disorder
Telangiectasia
hereditary hemorrhagic
Other Variants in ACVRL1