RS137852767 SDHA
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary cancer-predisposing syndrome
Dilated cardiomyopathy 1GG
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary cancer-predisposing syndrome
Dilated cardiomyopathy 1GG
Other Variants in SDHA