RS1800956 ENG

Health Risk Chr 9:127824342
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What This Variant Does
"rs1800956 (G/C transversion with D366H substitution) of endoglin may play an important role in the p...
Associated Conditions
Hereditary hemorrhagic telangiectasia
Telangiectasia
hereditary hemorrhagic
type 1
Hereditary hemorrhagic telangiectasia
Telangiectasia
hereditary hemorrhagic
type 1
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Endoglin levels — OR: 2.08 4E-29 PubMed
Other Variants in ENG
rs121918400 rs2131886961 rs2131875838 rs1564457752 rs267606783 rs121918401 rs121918402 rs150932144 rs373842615 rs730880096
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