RS770614769 OFD1

Health Risk Chr X:13746855
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Associated Conditions
Orofaciodigital syndrome I
Joubert syndrome 10
Retinitis pigmentosa 23
Simpson-Golabi-Behmel syndrome type 2
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
Orofaciodigital syndrome I
Joubert syndrome 10
Retinitis pigmentosa 23
Simpson-Golabi-Behmel syndrome type 2
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
Other Variants in OFD1
rs122460150 rs312262822 rs312262833 rs312262886 rs312262890 rs312262895 rs312262894 rs398122866 rs312262863 rs312262809
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