RS118192249 KCNQ3

Health Risk Chr 8:132175460 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Seizures
benign familial neonatal
2
Seizures
benign familial neonatal
2
Population Frequencies
gnomAD ALL
0%
Other Variants in KCNQ3
rs118192250 rs118192252 rs118192254 rs118192251 rs143224896 rs587781011 rs143683496 rs147173555 rs763446963 rs199682667
Ask Dr. Hemsworth about this variant