RS121908687 PLA2G6

Health Risk Chr 22:38112540 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive Parkinson disease 14
Infantile neuroaxonal dystrophy
Neurodegeneration with brain iron accumulation 2B
PLA2G6-associated neurodegeneration
Autosomal recessive Parkinson disease 14
Infantile neuroaxonal dystrophy
Neurodegeneration with brain iron accumulation 2B
PLA2G6-associated neurodegeneration
Population Frequencies
gnomAD ALL
0%
Other Variants in PLA2G6
rs121908680 rs121908681 rs121908682 rs587784343 rs121908683 rs587784353 rs121908685 rs121908686 rs387906863 rs387906864
Ask Dr. Hemsworth about this variant