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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTNS
(V257fs +1 more)
Duplication
(frameshift variant)
Inborn genetic diseases
+3 more
GPathogenic/Likely pathogenic
CTNS
(G149S +1 more)
Single nucleotide variant
(missense variant)
Ocular cystinosis
GUncertain significance