RS138772928 EIF2B5

Health Risk Chr 3:184144141 snv missense variant
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Associated Conditions
Vanishing white matter disease
Inborn genetic diseases
Vanishing white matter disease
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
0.1%
1kG EUR
100%
1kG SAS
100%
Other Variants in EIF2B5
rs28939717 rs28937596 rs113994074 rs113994049 rs113994054 rs113994061 rs113994055 rs113994053 rs113994064 rs113994043
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