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Links from MedGen

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP5F1A
(S99P +1 more)
Single nucleotide variant
(missense variant)
Combined oxidative phosphorylation deficiency 22
+1 more
GUncertain significance
ATP5F1A
Single nucleotide variant
(splice donor variant)
not provided
+1 more
GLikely pathogenic
ATP5F1A
(Y321C +2 more)
Single nucleotide variant
(missense variant)
Combined oxidative phosphorylation deficiency 22
GPathogenic
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