RS766413410 AGK

Health Risk Chr 7:141615468
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cataract 38
Sengers syndrome
Autosomal recessive AGK-related phenotype
Inborn genetic diseases
Cataract 38
Sengers syndrome
Autosomal recessive AGK-related phenotype
Inborn genetic diseases
Other Variants in AGK
rs1554399572 rs1554405935 rs868431923 rs387907024 rs1554401641 rs387907025 rs771945804 rs542547163 rs41275003 rs746709222
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