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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MID1
(R434H +1 more)
Single nucleotide variant
(missense variant)
X-linked Opitz G/BBB syndrome
GUncertain significance
MID1
(I193M +1 more)
Single nucleotide variant
(missense variant)
X-linked Opitz G/BBB syndrome
GUncertain significance