RS886039773 SON

Health Risk Chr 21:33554982
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What This Variant Does
"CLNSIG=5
Associated Conditions
ZTTK syndrome
Failure to thrive
Global developmental delay
Inborn genetic diseases
Neurodevelopmental abnormality
Hereditary spastic paraplegia 17
See cases
ZTTK syndrome
Failure to thrive
Global developmental delay
Inborn genetic diseases
Neurodevelopmental abnormality
Hereditary spastic paraplegia 17
See cases
Other Variants in SON
rs886039777 rs886039778 rs1114167303 rs886039779 rs886039774 rs886039775 rs886039776 rs886041970 rs1064796472 rs1131691911
Ask Dr. Hemsworth about this variant