RS139334167 SPG11

Health Risk Chr 15:44564628 snv missense variant
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Associated Conditions
Hereditary spastic paraplegia 11
Hereditary spastic paraplegia
Inborn genetic diseases
SPG11-related disorder
Hereditary spastic paraplegia 11
Hereditary spastic paraplegia
Inborn genetic diseases
SPG11-related disorder
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
100%
1kG ALL
99.8%
1kG AMR
99.3%
1kG EAS
100%
1kG EUR
99.6%
1kG SAS
100%
Other Variants in SPG11
rs118203963 rs312262716 rs267607084 rs312262720 rs312262744 rs312262715 rs200079802 rs141848292 rs312262752 rs312262722
Ask Dr. Hemsworth about this variant