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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYLD-AS1, NOD2
(N1010S +1 more)
Single nucleotide variant
(missense variant +1 more)
NOD2-related disorder
+2 more
GUncertain significance
CYLD-AS1, NOD2
Single nucleotide variant
(synonymous variant +1 more)
NOD2-related disorder
+3 more
GLikely benign
CYLD-AS1, NOD2
Single nucleotide variant
(synonymous variant +1 more)
NOD2-related disorder
GLikely benign
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