RS121912678 ACVR1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Progressive myositis ossificans
Inborn genetic diseases
Epicanthus
ACVR1-related disorder
Ependymoma
Diffuse pediatric-type high-grade glioma
H3-wildtype and IDH-wildtype
Diffuse midline glioma
H3 K27M-mutant
Progressive myositis ossificans
Inborn genetic diseases
Epicanthus
ACVR1-related disorder
Ependymoma
Diffuse pediatric-type high-grade glioma
Other Variants in ACVR1