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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFRD1
(I172V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
IFRD1
Duplication
(intron variant)
IFRD1-related disorder
GLikely benign