RS1064794218 ENG

Health Risk Chr 9:127818149
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What This Variant Does
"CLNSIG=4
Associated Conditions
Cardiovascular phenotype
Hereditary hemorrhagic telangiectasia
Cardiovascular phenotype
Hereditary hemorrhagic telangiectasia
Other Variants in ENG
rs121918400 rs2131886961 rs2131875838 rs1564457752 rs267606783 rs121918401 rs121918402 rs150932144 rs373842615 rs730880096
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