RS753385776 PIGW
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Global developmental delay
Cleft palate
Abnormal skeletal morphology
Hyperphosphatasia with intellectual disability syndrome 5
Inborn genetic diseases
Global developmental delay
Cleft palate
Abnormal skeletal morphology
Hyperphosphatasia with intellectual disability syndrome 5
Inborn genetic diseases
Other Variants in PIGW