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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SH3PXD2B
(P730L)
Single nucleotide variant
(missense variant +1 more)
Frank-Ter Haar syndrome
+2 more
GConflicting classifications of pathogenicity
SH3PXD2B
(R698Q)
Single nucleotide variant
(missense variant +1 more)
Frank-Ter Haar syndrome
+1 more
GUncertain significance
SH3PXD2B
(R539W)
Single nucleotide variant
(missense variant +1 more)
Frank-Ter Haar syndrome
+1 more
GConflicting classifications of pathogenicity
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