RS199894905 SLC25A15
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Inborn genetic diseases
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Inborn genetic diseases
Other Variants in SLC25A15