RS121918620 ATP1A2

Health Risk Chr 1:160128760 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Migraine
familial hemiplegic
2
Familial hemiplegic migraine
Inborn genetic diseases
Familial hemiplegic migraine
Migraine
familial hemiplegic
2
Familial hemiplegic migraine
Inborn genetic diseases
Familial hemiplegic migraine
Population Frequencies
gnomAD ALL
0%
Other Variants in ATP1A2
rs28933398 rs28933399 rs28933400 rs28933401 rs28934002 rs121918612 rs121918613 rs121918614 rs121918615 rs121918616
Ask Dr. Hemsworth about this variant