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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYNJ1
(P1121T +2 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 53
+1 more
GUncertain significance
SYNJ1
(S1072P +2 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
SYNJ1
(R549H +2 more)
Single nucleotide variant
(missense variant)
Early-onset Parkinson disease 20
+1 more
GUncertain significance
SYNJ1
(C21G)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 53
+1 more
GUncertain significance
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