RS140430952 TGDS

Health Risk Chr 13:94590868
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What This Variant Does
"CLNSIG=5
Associated Conditions
Catel-Manzke syndrome
Inborn genetic diseases
TGDS-related disorder
Catel-Manzke syndrome
Inborn genetic diseases
TGDS-related disorder
Other Variants in TGDS
rs544436734 rs724160004 rs727502808 rs727502809 rs724160005 rs1888779255 rs1889172738 rs775273838 rs2501948490
Ask Dr. Hemsworth about this variant