RS797044883 MAGEL2

Health Risk Chr 15:23645831
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Schaaf-Yang syndrome
Prader-Willi syndrome
MAGEL2-related disorder
Inborn genetic diseases
Schaaf-Yang syndrome
Prader-Willi syndrome
MAGEL2-related disorder
Other Variants in MAGEL2
rs398122415 rs398122416 rs398122417 rs398122418 rs770374710 rs2233061 rs760039339 rs794726941 rs146970674 rs781777662
Ask Dr. Hemsworth about this variant