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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A24
Deletion
(splice donor variant)
Fontaine progeroid syndrome
GUncertain significance
SLC25A24
(R198C +1 more)
Single nucleotide variant
(missense variant)
Fontaine progeroid syndrome
+1 more
GPathogenic