RS2275402 EMC1

Health Risk Chr 1:19230900
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Associated Conditions
Retinal dystrophy
Inborn genetic diseases
Cerebellar atrophy
visual impairment
and psychomotor retardation
Retinal dystrophy
Inborn genetic diseases
Cerebellar atrophy
visual impairment
and psychomotor retardation
Other Variants in EMC1
rs869320624 rs879253819 rs869320625 rs869320623 rs751484278 rs1553252938 rs781137936 rs1558096194 rs901905420 rs148538980
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