RS763735590 CC2D2A
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Joubert syndrome 9
Meckel-Gruber syndrome
Joubert syndrome
Inborn genetic diseases
Joubert syndrome 9
Meckel-Gruber syndrome
Joubert syndrome
Inborn genetic diseases
Other Variants in CC2D2A