RS113994016 EIF2B2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Premature ovarian insufficiency
Vanishing white matter disease
Osteogenesis imperfecta
Leukoencephalopathy with vanishing white matter 2
Premature ovarian insufficiency
Vanishing white matter disease
Osteogenesis imperfecta
Leukoencephalopathy with vanishing white matter 2
Other Variants in EIF2B2