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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LTBP4
(V125M +2 more)
Single nucleotide variant
(missense variant)
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
GUncertain significance
LTBP4
(G416R +2 more)
Single nucleotide variant
(missense variant)
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
+1 more
GConflicting classifications of pathogenicity