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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POC1B
(S279P +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
POC1B
(R80* +1 more)
Single nucleotide variant
(nonsense)
Retinal dystrophy
+1 more
GPathogenic/Likely pathogenic