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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRIP11
(I1363V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TRIP11
(E712K +1 more)
Single nucleotide variant
(missense variant)
Connective tissue disorder
+4 more
GBenign/Likely benign