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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2D
(R5340*)
Single nucleotide variant
(nonsense)
Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome
+4 more
GPathogenic
KMT2D
(P2662fs)
Deletion
(frameshift variant)
Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome
+1 more
GPathogenic