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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NRL
(R31*)
Single nucleotide variant
(nonsense +1 more)
Retinitis pigmentosa 27
+1 more
GPathogenic/Likely pathogenic
NRL, PCK2
(R469C +1 more)
Single nucleotide variant
(missense variant +1 more)
Phosphoenolpyruvate carboxykinase deficiency, mitochondrial
+1 more
GConflicting classifications of pathogenicity