RS770374710 MAGEL2

Health Risk Chr 15:23645747
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What This Variant Does
"CLNSIG=5
Associated Conditions
Schaaf-Yang syndrome
Inborn genetic diseases
Neurodevelopmental delay
See cases
Neurodevelopmental disorder
Prader-Willi-like syndrome
Schaaf-Yang syndrome
Ventriculomegaly
Multiple joint contractures
Generalized hypotonia
Ambiguous genitalia
Schaaf-Yang syndrome
Inborn genetic diseases
Neurodevelopmental delay
See cases
Other Variants in MAGEL2
rs398122415 rs398122416 rs398122417 rs398122418 rs2233061 rs760039339 rs794726941 rs146970674 rs781777662 rs541262134
Ask Dr. Hemsworth about this variant