RS116134953 SLC25A22

Health Risk Chr 11:794508 snv missense variant
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Associated Conditions
Early myoclonic encephalopathy
Inborn genetic diseases
SLC25A22-related disorder
Early-infantile DEE
Early myoclonic encephalopathy
Inborn genetic diseases
SLC25A22-related disorder
Early-infantile DEE
Population Frequencies
gnomAD ALL
0%
1kG AFR
1.1%
1kG ALL
0.3%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
99.9%
Other Variants in SLC25A22
rs121918334 rs121918335 rs587777243 rs587781167 rs146402942 rs141975755 rs587781169 rs376015598 rs374780430 rs145322467
Ask Dr. Hemsworth about this variant