RS779485996 ACVRL1

Health Risk Chr 12:51915293
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What This Variant Does
"CLNSIG=5
Associated Conditions
Telangiectasia
hereditary hemorrhagic
type 2
ACVRL1-related disorder
Cardiovascular phenotype
Telangiectasia
hereditary hemorrhagic
type 2
ACVRL1-related disorder
Cardiovascular phenotype
Other Variants in ACVRL1
rs121909284 rs28936399 rs121909285 rs387906392 rs121909286 rs28936401 rs387906393 rs121909287 rs121909288 rs28936687
Ask Dr. Hemsworth about this variant