RS797044903 PLA2G6

Health Risk Chr 22:38132883
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Infantile neuroaxonal dystrophy
Neurodegeneration with brain iron accumulation 2B
Autosomal recessive Parkinson disease 14
Inborn genetic diseases
Infantile neuroaxonal dystrophy
Neurodegeneration with brain iron accumulation 2B
Autosomal recessive Parkinson disease 14
Other Variants in PLA2G6
rs121908680 rs121908681 rs121908682 rs587784343 rs121908683 rs587784353 rs121908685 rs121908686 rs121908687 rs387906863
Ask Dr. Hemsworth about this variant