RS139631202 TRAPPC9

Health Risk Chr 8:140451110 snv missense variant
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Associated Conditions
Intellectual disability
autosomal recessive 13
Inborn genetic diseases
TRAPPC9-related disorder
Intellectual disability
autosomal recessive 13
Inborn genetic diseases
TRAPPC9-related disorder
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
99.9%
1kG EUR
99.9%
1kG SAS
100%
Other Variants in TRAPPC9
rs267607136 rs267607137 rs2131714307 rs1587520018 rs146235874 rs587780484 rs587780485 rs587780486 rs786205595 rs150200902
Ask Dr. Hemsworth about this variant