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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DENND3
(K720fs +1 more)
Deletion
(frameshift variant +1 more)
Hirschsprung disease, susceptibility to, 1
GLikely pathogenic
NUP98
(N1662S +6 more)
Single nucleotide variant
(missense variant +1 more)
Hirschsprung disease, susceptibility to, 1
GLikely pathogenic
NCLN
(Q166*)
Single nucleotide variant
(nonsense)
Hirschsprung disease, susceptibility to, 1
GLikely pathogenic
TBATA
(R53C)
Single nucleotide variant
(missense variant +1 more)
Hirschsprung disease, susceptibility to, 1
GLikely pathogenic
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