RS398122366 TTI2

Health Risk Chr 8:33503763
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome
Inborn genetic diseases
Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome
Inborn genetic diseases
Other Variants in TTI2
rs398122367 rs3736497 rs199720231 rs138108276 rs758541435 rs1809594670 rs138419634 rs200045967 rs765235179 rs1180962073
Ask Dr. Hemsworth about this variant