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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NUBPL
(V182A +1 more)
Single nucleotide variant
(missense variant +1 more)
NUBPL-related condition
+2 more
GConflicting classifications of pathogenicity
NDUFAF5
(K109N)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
+2 more
GPathogenic/Likely pathogenic