RS863225296 ANKRD11;TRAPPC2L
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What This Variant Does
"CLNSIG=5
Associated Conditions
KBG syndrome
Encephalopathy
progressive
early-onset
with episodic rhabdomyolysis
Inborn genetic diseases
KBG syndrome
Encephalopathy
progressive
early-onset
with episodic rhabdomyolysis
Inborn genetic diseases
Other Variants in ANKRD11;TRAPPC2L