RS756431692 MCM3AP

Health Risk Chr 21:46260897
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Associated Conditions
Peripheral neuropathy
autosomal recessive
with or without impaired intellectual development
Inborn genetic diseases
MCM3AP-related disorder
Peripheral neuropathy
autosomal recessive
with or without impaired intellectual development
Inborn genetic diseases
MCM3AP-related disorder
Other Variants in MCM3AP
rs483352869 rs779248881 rs1569086477 rs1569073058 rs1569074992 rs373674344 rs1569072024 rs1569074977 rs763090302 rs1218260846
Ask Dr. Hemsworth about this variant