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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL27A1
(R707*)
Single nucleotide variant
(nonsense)
Steel syndrome
+1 more
GPathogenic
COL27A1
Single nucleotide variant
(splice acceptor variant)
Steel syndrome
GPathogenic
COL27A1
(P1615L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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