RS121918616 ATP1A2

Health Risk Chr 1:160130283
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Migraine
familial basilar
Familial hemiplegic migraine
familial hemiplegic
2
ATP1A2-related disorder
Developmental and epileptic encephalopathy 98
Migraine
familial basilar
Familial hemiplegic migraine
familial hemiplegic
2
ATP1A2-related disorder
Developmental and epileptic encephalopathy 98
Other Variants in ATP1A2
rs28933398 rs28933399 rs28933400 rs28933401 rs28934002 rs121918612 rs121918613 rs121918614 rs121918615 rs121918617
Ask Dr. Hemsworth about this variant