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Links from MedGen

Items: 1 to 100 of 428

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNA5
(R250W)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(P294S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A60S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(V476I)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(M1T)
Single nucleotide variant
(missense variant +1 more)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(V259I)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(E208K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(G385E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R403L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(T607S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(I489M)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(G567E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(V556F)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(G19D)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(T15I)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(A209V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(V64M)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(E211K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A298fs)
Deletion
(frameshift variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(S395F)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(P77A)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(L315P)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(T39K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(P82S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(T271N)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(G53E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(M357T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(E48K)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(T15A)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(K585N)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A397T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A56V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(N299K)
Single nucleotide variant
(missense variant)
KCNA5-related disorder
+1 more
GUncertain significance
KCNA5
(A4S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(G174A)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GConflicting classifications of pathogenicity
KCNA5
(S171N)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA1, KCNA5
Duplication
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(V107G)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R212H)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GUncertain significance
KCNA5
(P37L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
+1 more
GUncertain significance
KCNA5
(P228H)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(S557fs)
Duplication
(frameshift variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(I515V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A590V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(P7R)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(P69L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(L372V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
KCNA5
(L320P)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R201L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(D207E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(E538Q)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A287E)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(I126T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(T336S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(A470T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(Y179H)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A56S)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A139V)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(R90L)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(P82T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(L78F)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(A50T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
(K565Q)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
KCNA5
(V594M)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 7
GUncertain significance
KCNA5
Single nucleotide variant
(synonymous variant)
Atrial fibrillation, familial, 7
GLikely benign
Display optionsSort by RelevanceDownload
Format
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