RS121909120 TCF4

Health Risk Chr 18:55228988
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What This Variant Does
"[OMIM:?]
Associated Conditions
Pitt-Hopkins syndrome
Severe intellectual deficiency
Inborn genetic diseases
Pitt-Hopkins syndrome
Severe intellectual deficiency
Inborn genetic diseases
Other Variants in TCF4
rs121909121 rs121909122 rs121909123 rs1600861681 rs398123560 rs398123561 rs587784462 rs587784460 rs587784459 rs587784458
Ask Dr. Hemsworth about this variant