RS121909123 TCF4

Health Risk Chr 18:55228993
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What This Variant Does
"[OMIM:?]
Associated Conditions
Pitt-Hopkins syndrome
Pitt-Hopkins syndrome
Microcephaly
Inborn genetic diseases
TCF4-related disorder
Corneal dystrophy
Fuchs endothelial
3
Pitt-Hopkins syndrome
Pitt-Hopkins syndrome
Microcephaly
Inborn genetic diseases
TCF4-related disorder
Corneal dystrophy
Fuchs endothelial
Other Variants in TCF4
rs121909120 rs121909121 rs121909122 rs1600861681 rs398123560 rs398123561 rs587784462 rs587784460 rs587784459 rs587784458
Ask Dr. Hemsworth about this variant