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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUL7
(Y1021D +1 more)
Single nucleotide variant
(missense variant)
3M syndrome 1
GLikely pathogenic
CUL7
(R550* +2 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic