RS118192218 KCNQ2

Health Risk Chr 20:63433869 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Seizures
benign familial neonatal
1
Early-infantile DEE
Seizures
benign familial neonatal
1
Early-infantile DEE
Seizures
benign familial neonatal
1
Early-infantile DEE
Seizures
benign familial neonatal
1
Other Variants in KCNQ2
rs28939683 rs74315390 rs28939684 rs74315391 rs267607198 rs74315392 rs118192244 rs118192200 rs118192217 rs118192219
Ask Dr. Hemsworth about this variant