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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYN1
(P655L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SYN1
(T567A)
Single nucleotide variant
(missense variant)
SYN1-related condition
+4 more
GConflicting classifications of pathogenicity
SYN1
(G539S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
SYN1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SYN1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
SYN1
(L442P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
SYN1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
SYN1
Deletion
(intron variant)
SYN1-related condition
+3 more
GBenign
SYN1
Single nucleotide variant
(synonymous variant)
History of neurodevelopmental disorder
+4 more
GBenign
SYN1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
SYN1
(W126*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
SYN1
(T124I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
SYN1
(A106S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SYN1
(A51G)
Single nucleotide variant
(missense variant)
History of neurodevelopmental disorder
+3 more
GBenign
SYN1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
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