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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DLG3
(T66I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DLG3
(G102S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GBenign
DLG3
Single nucleotide variant
(intron variant)
not specified
GBenign
DLG3
Single nucleotide variant
(intron variant)
DLG3-related condition
+3 more
GBenign/Likely benign
DLG3
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
DLG3
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DLG3
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
+1 more
GBenign
DLG3
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
DLG3
(Y760* +2 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
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