RS886039530 ATP1A2

Health Risk Chr 1:160130547
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What This Variant Does
"CLNSIG=5
Associated Conditions
Epileptic encephalopathy
Familial hemiplegic migraine
Inborn genetic diseases
Migraine
familial hemiplegic
2
Epileptic encephalopathy
Familial hemiplegic migraine
Inborn genetic diseases
Migraine
familial hemiplegic
2
Other Variants in ATP1A2
rs28933398 rs28933399 rs28933400 rs28933401 rs28934002 rs121918612 rs121918613 rs121918614 rs121918615 rs121918616
Ask Dr. Hemsworth about this variant