RS730880016 TCF12

Health Risk Chr 15:57273122
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What This Variant Does
"CLNSIG=5
Associated Conditions
TCF12-related craniosynostosis
Inborn genetic diseases
TCF12-related craniosynostosis
Inborn genetic diseases
Other Variants in TCF12
rs886037636 rs886037637 rs398122381 rs886037638 rs886037639 rs886037640 rs886037641 rs730880017 rs730880015 rs730880326
Ask Dr. Hemsworth about this variant