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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AIFM1, RAB33A
Single nucleotide variant
(synonymous variant +2 more)
AIFM1-related condition
+6 more
GBenign/Likely benign
AIFM1, RAB33A
(A318T +1 more)
Single nucleotide variant
(missense variant +1 more)
Combined oxidative phosphorylation deficiency
+2 more
GConflicting classifications of pathogenicity