RS398123561 TCF4

Health Risk Chr 18:55350391
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
Pitt-Hopkins syndrome
Neurodevelopmental disorder
Intellectual disability
Pitt-Hopkins syndrome
Neurodevelopmental disorder
Other Variants in TCF4
rs121909120 rs121909121 rs121909122 rs121909123 rs1600861681 rs398123560 rs587784462 rs587784460 rs587784459 rs587784458
Ask Dr. Hemsworth about this variant