RS869320625 EMC1

Health Risk Chr 1:19243991
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cerebellar atrophy
visual impairment
and psychomotor retardation
Inborn genetic diseases
EMC1-related disorder
Cerebellar atrophy
visual impairment
and psychomotor retardation
Inborn genetic diseases
EMC1-related disorder
Other Variants in EMC1
rs869320624 rs879253819 rs869320623 rs751484278 rs1553252938 rs781137936 rs1558096194 rs901905420 rs148538980 rs778470143
Ask Dr. Hemsworth about this variant