RS142441643 SDHA
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 5
Carney triad
Mitochondrial complex II deficiency
nuclear type 1
Pilocytic astrocytoma
Leigh syndrome
Rhabdomyosarcoma
Gastrointestinal stromal tumor
Dilated cardiomyopathy 1GG
Neurodegeneration with ataxia and late-onset optic atrophy
SDHA-related disorder
Inherited phaeochromocytoma and paraganglioma excluding NF1
Intellectual disability
Hereditary pheochromocytoma and paraganglioma
Other Variants in SDHA