RS138852641 KCNQ3

Health Risk Chr 8:132129542 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Benign neonatal seizures
Seizures
benign familial neonatal
2
Inborn genetic diseases
Benign neonatal seizures
Seizures
benign familial neonatal
2
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.9%
1kG SAS
100%
Other Variants in KCNQ3
rs118192250 rs118192252 rs118192254 rs118192249 rs118192251 rs143224896 rs587781011 rs143683496 rs147173555 rs763446963
Ask Dr. Hemsworth about this variant