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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HOXB13
(R258H)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
HOXB13
(P32H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance