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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNQ3
(N821S +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
KCNQ3
Single nucleotide variant
(synonymous variant)
Benign neonatal seizures
+1 more
GConflicting classifications of pathogenicity
KCNQ3
(R777Q +1 more)
Single nucleotide variant
(missense variant)
Seizures, benign familial neonatal, 2
+3 more
GConflicting classifications of pathogenicity
KCNQ3
(S665L +1 more)
Single nucleotide variant
(missense variant)
Benign neonatal seizures
+3 more
GConflicting classifications of pathogenicity
KCNQ3
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
KCNQ3
Single nucleotide variant
(synonymous variant)
KCNQ3-related condition
+4 more
GBenign/Likely benign
KCNQ3
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
KCNQ3
(P574S +1 more)
Single nucleotide variant
(missense variant)
KCNQ3-related condition
+7 more
GBenign/Likely benign
KCNQ3
(V522I +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
KCNQ3
(L515V +1 more)
Single nucleotide variant
(missense variant)
Benign neonatal seizures
+1 more
GUncertain significance
KCNQ3
(D510A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNQ3
(S486R +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KCNQ3
(N468S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
KCNQ3
(P409R +1 more)
Single nucleotide variant
(missense variant)
Seizures, benign familial neonatal, 2
+2 more
GConflicting classifications of pathogenicity
KCNQ3
Single nucleotide variant
(synonymous variant)
Benign neonatal seizures
+2 more
GConflicting classifications of pathogenicity
KCNQ3
Single nucleotide variant
(synonymous variant)
Benign neonatal seizures
+1 more
GConflicting classifications of pathogenicity
KCNQ3
(T263M +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KCNQ3
Single nucleotide variant
(intron variant)
not provided
+2 more
GConflicting classifications of pathogenicity
KCNQ3
(Q52E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNQ3
(V43M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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