RS794729225 CC2D2A

Health Risk Chr 4:15587843
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Joubert syndrome 1
Joubert syndrome
Meckel-Gruber syndrome
CC2D2A-related disorder
Inborn genetic diseases
Joubert syndrome 1
Joubert syndrome
Meckel-Gruber syndrome
CC2D2A-related disorder
Other Variants in CC2D2A
rs2109050324 rs116358011 rs118204051 rs118204052 rs118204053 rs386833750 rs267606709 rs387907058 rs386833745 rs386833746
Ask Dr. Hemsworth about this variant