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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MID1
(W399* +1 more)
Single nucleotide variant
(nonsense)
X-linked Opitz G/BBB syndrome
GLikely pathogenic
MID1
(R219S +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity