RS762633090 CEP290
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Associated Conditions
Retinal dystrophy
Nephronophthisis
Joubert syndrome
Meckel-Gruber syndrome
Leber congenital amaurosis
Bardet-Biedl syndrome 14
Meckel syndrome
type 4
Inborn genetic diseases
Retinal dystrophy
Nephronophthisis
Joubert syndrome
Meckel-Gruber syndrome
Leber congenital amaurosis
Bardet-Biedl syndrome 14
Other Variants in CEP290