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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GABBR2
Single nucleotide variant
(intron variant)
Neurodevelopmental disorder with poor language and loss of hand skills
+3 more
GConflicting classifications of pathogenicity
GABBR2
(R44Q)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with poor language and loss of hand skills
+4 more
GUncertain significance
GABBR2
(G41C)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
+3 more
GUncertain significance
RYR3
(R308Q)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
RYR3
(A3807E +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
RYR3
(D4349Y +1 more)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
GUncertain significance
FASN
(V2058M)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
GUncertain significance
FASN
(A847T)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
GUncertain significance
FASN
(R490C)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
FASN
(A342S)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
+1 more
GUncertain significance
FASN
(S279L)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
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