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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL9A2
(P661L)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
COL9A2
(P661T)
Single nucleotide variant
(missense variant)
Connective tissue disorder
+3 more
GBenign/Likely benign
COL9A2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GLikely benign
COL9A2
(Q467R)
Single nucleotide variant
(missense variant)
Stickler syndrome, type 5
+3 more
GConflicting classifications of pathogenicity
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