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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SP7
(V307I +1 more)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type 12
GUncertain significance
SP7
(G134A +1 more)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type 12
GUncertain significance
FKBP10
(G278fs)
Duplication
(frameshift variant)
Abnormality of the skeletal system
+6 more
GConflicting classifications of pathogenicity
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