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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNGB1
(N986I +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
CNGB1
(W919* +1 more)
Single nucleotide variant
(nonsense)
Retinitis pigmentosa 45
+1 more
GPathogenic
CNGB1
(W4*)
Single nucleotide variant
(nonsense)
not specified
+3 more
GConflicting classifications of pathogenicity
CNGB1
(M1I)
Single nucleotide variant
(missense variant +1 more)
Retinitis pigmentosa 45
+2 more
GUncertain significance
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