RS1064794848 HK1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Neurodevelopmental disorder with visual defects and brain anomalies
Retinitis pigmentosa
Retinitis pigmentosa 79
Inborn genetic diseases
Hemolytic anemia due to hexokinase deficiency
Autism spectrum disorder
Retinal dystrophy
Neurodevelopmental disorder with visual defects and brain anomalies
Retinitis pigmentosa
Retinitis pigmentosa 79
Inborn genetic diseases
Hemolytic anemia due to hexokinase deficiency
Autism spectrum disorder
Retinal dystrophy
Other Variants in HK1