RS864321624 SLC25A42
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn mitochondrial myopathy
Metabolic crises
recurrent
with variable encephalomyopathic features and neurologic regression
SLC25A42-related mitochondrial disorder
Inborn mitochondrial myopathy
Metabolic crises
recurrent
with variable encephalomyopathic features and neurologic regression
SLC25A42-related mitochondrial disorder
Other Variants in SLC25A42