RS797044875 CTNNB1

Health Risk Chr 3:41235763
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Severe intellectual disability-progressive spastic diplegia syndrome
CTNNB1-related disorder
Inborn genetic diseases
Severe intellectual disability-progressive spastic diplegia syndrome
CTNNB1-related disorder
Other Variants in CTNNB1
rs587776850 rs121913400 rs121913396 rs121913403 rs121913412 rs28931588 rs28931589 rs121913413 rs121913409 rs121913407
Ask Dr. Hemsworth about this variant