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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTC19, LOC130060312
Duplication
(3 prime UTR variant)
Mitochondrial complex III deficiency nuclear type 1
GUncertain significance
LOC130060312, TTC19
Single nucleotide variant
(3 prime UTR variant)
Mitochondrial complex III deficiency nuclear type 2
GUncertain significance
LOC130060312, TTC19
Single nucleotide variant
(3 prime UTR variant)
Mitochondrial complex III deficiency nuclear type 2
GLikely benign
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