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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM111A
(S178L)
Single nucleotide variant
(missense variant)
Osteocraniostenosis
GUncertain significance
FAM111A
(M606I)
Single nucleotide variant
(missense variant)
Osteocraniostenosis
GUncertain significance