RS755348996 ENG
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary hemorrhagic telangiectasia
See cases
Cardiovascular phenotype
Telangiectasia
hereditary hemorrhagic
type 1
ENG-related disorder
Hereditary hemorrhagic telangiectasia
See cases
Cardiovascular phenotype
Telangiectasia
hereditary hemorrhagic
type 1
ENG-related disorder
Other Variants in ENG