RS118192252 KCNQ3

Health Risk Chr 8:132141190 snv missense variant
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What This Variant Does
"CLNSIG=5
Associated Conditions
Seizures
benign familial neonatal
2
Benign neonatal seizures
Inborn genetic diseases
Seizures
benign familial neonatal
2
Benign neonatal seizures
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
1kG AFR
100%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
99.8%
1kG EUR
100%
1kG SAS
99.9%
Other Variants in KCNQ3
rs118192250 rs118192254 rs118192249 rs118192251 rs143224896 rs587781011 rs143683496 rs147173555 rs763446963 rs199682667
Ask Dr. Hemsworth about this variant