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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HOXD13
(G237R)
Single nucleotide variant
(missense variant)
Synpolydactyly type 1
GUncertain significance
HOXD13
(R274*)
Single nucleotide variant
(nonsense)
not provided
+13 more
GPathogenic/Likely pathogenic