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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UCP3
(R143*)
Single nucleotide variant
(nonsense)
UCP3-related disorder
+2 more
GConflicting classifications of pathogenicity
UCP3
(R70W)
Single nucleotide variant
(missense variant)
UCP3-related disorder
+2 more
GUncertain significance