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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LYRM7
Deletion
not provided
GPathogenic
LYRM7
(N43S)
Single nucleotide variant
(missense variant)
Mitochondrial complex III deficiency nuclear type 8
GUncertain significance
LYRM7
Single nucleotide variant
(splice acceptor variant)
Mitochondrial complex III deficiency nuclear type 1
GPathogenic
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