RS121908683 PLA2G6
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What This Variant Does
"[OMIM:?]
Associated Conditions
Karak syndrome
Neurodegeneration with brain iron accumulation
PLA2G6-associated neurodegeneration
Infantile neuroaxonal dystrophy
Autosomal recessive Parkinson disease 14
Neurodegeneration with brain iron accumulation 2B
Karak syndrome
Neurodegeneration with brain iron accumulation
PLA2G6-associated neurodegeneration
Infantile neuroaxonal dystrophy
Autosomal recessive Parkinson disease 14
Neurodegeneration with brain iron accumulation 2B
Other Variants in PLA2G6