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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SP7
(D102fs +1 more)
Deletion
(frameshift variant)
Osteogenesis imperfecta type 12
GLikely pathogenic
SP7
(G134A +1 more)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type 12
GUncertain significance
SP7
(V307I +1 more)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type 12
GUncertain significance
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