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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A42
(V194M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130064046, SLC25A42
(R222P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance