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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LYRM7
(M1T)
Single nucleotide variant
(missense variant +2 more)
Mitochondrial complex III deficiency nuclear type 8
GPathogenic/Likely pathogenic
LYRM7
(N43S)
Single nucleotide variant
(missense variant)
Mitochondrial complex III deficiency nuclear type 8
GUncertain significance
LYRM7
(S49del)
Microsatellite
(inframe_deletion)
not provided
+1 more
GUncertain significance
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