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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GPC3
Single nucleotide variant
(intron variant)
Simpson-Golabi-Behmel syndrome type 1
GUncertain significance
GPC3
Single nucleotide variant
(splice acceptor variant)
Simpson-Golabi-Behmel syndrome type 1
GLikely pathogenic
GPC3
(P131S +2 more)
Single nucleotide variant
(missense variant)
Simpson-Golabi-Behmel syndrome type 1
GUncertain significance
GPC3
(N162S +2 more)
Single nucleotide variant
(missense variant)
Wilms tumor 1
+4 more
GConflicting classifications of pathogenicity
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