RS1057518848 TCF4

Health Risk Chr 18:55229003
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What This Variant Does
"CLNSIG=5
Associated Conditions
Global developmental delay
Cerebral hypoplasia
Pitt-Hopkins syndrome
Global developmental delay
Cerebral hypoplasia
Pitt-Hopkins syndrome
Other Variants in TCF4
rs121909120 rs121909121 rs121909122 rs121909123 rs1600861681 rs398123560 rs398123561 rs587784462 rs587784460 rs587784459
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