RS9697983 GLUD2

Health Risk Chr X:121049175 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Parkinson disease
late-onset
See cases
GLUD2-related disorder
Parkinson disease
late-onset
See cases
GLUD2-related disorder
Population Frequencies
gnomAD ALL
2.6%
1kG AFR
93.1%
1kG ALL
3.3%
1kG AMR
2.1%
1kG EAS
100%
1kG EUR
2.6%
1kG SAS
96.7%
Other Variants in GLUD2
rs199547711 rs756544884 rs140532390
Ask Dr. Hemsworth about this variant