RS1060503237 ACVRL1

Health Risk Chr 12:51920758
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What This Variant Does
"CLNSIG=4
Associated Conditions
Telangiectasia
hereditary hemorrhagic
type 2
Cardiovascular phenotype
Telangiectasia
hereditary hemorrhagic
type 2
Cardiovascular phenotype
Other Variants in ACVRL1
rs121909284 rs28936399 rs121909285 rs387906392 rs121909286 rs28936401 rs387906393 rs121909287 rs121909288 rs28936687
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