RS144088322 MAP1B

Health Risk Chr 5:72196356
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Associated Conditions
Inborn genetic diseases
Hearing loss
autosomal dominant 83
Periventricular nodular heterotopia 9
Inborn genetic diseases
Hearing loss
autosomal dominant 83
Periventricular nodular heterotopia 9
Other Variants in MAP1B
rs1554054827 rs1554054831 rs1554054880 rs1554055106 rs1580027036 rs1561314246 rs1561315170 rs1580026238 rs1747146910 rs371409009
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