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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HOXD13
(R306W)
Single nucleotide variant
(missense variant)
Synpolydactyly type 1
+1 more
GPathogenic/Likely pathogenic
HOXD13
(S316C)
Single nucleotide variant
(missense variant)
Brachydactyly type D
+1 more
GPathogenic
HOXD13
(I322L)
Single nucleotide variant
(missense variant)
Brachydactyly type D
+1 more
GPathogenic
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