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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TGFB2
(P119L +1 more)
Single nucleotide variant
(missense variant +1 more)
Ehlers-Danlos syndrome
+5 more
GConflicting classifications of pathogenicity
ESRRG, GPATCH2
+4 more
Copy number loss
Scoliosis
+4 more
GPathogenic