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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EXOC7
Single nucleotide variant
(intron variant)
not provided
+2 more
GLikely benign
EXOC7
(S153*)
Single nucleotide variant
(nonsense +1 more)
See cases
+2 more
GBenign