RS767230468 ATP1A2

Health Risk Chr 1:160130136
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Associated Conditions
Familial hemiplegic migraine
Inborn genetic diseases
Familial hemiplegic migraine
Inborn genetic diseases
Other Variants in ATP1A2
rs28933398 rs28933399 rs28933400 rs28933401 rs28934002 rs121918612 rs121918613 rs121918614 rs121918615 rs121918616
Ask Dr. Hemsworth about this variant