RS1057521070 TCF4

Health Risk Chr 18:55228999
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Pitt-Hopkins syndrome
TCF4-related disorder
Medulloblastoma SHH activated
Pitt-Hopkins syndrome
Inborn genetic diseases
Pitt-Hopkins syndrome
TCF4-related disorder
Medulloblastoma SHH activated
Pitt-Hopkins syndrome
Other Variants in TCF4
rs121909120 rs121909121 rs121909122 rs121909123 rs1600861681 rs398123560 rs398123561 rs587784462 rs587784460 rs587784459
Ask Dr. Hemsworth about this variant