RS869320802 CTBP1

Health Risk Chr 4:1213028
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypotonia
ataxia
developmental delay
and tooth enamel defect syndrome
Inborn genetic diseases
Hypotonia
ataxia
developmental delay
and tooth enamel defect syndrome
Inborn genetic diseases
Other Variants in CTBP1
rs1731781760 rs374755819 rs767549924 rs199614101 rs750734000 rs750112627
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