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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TULP1
(F453L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TULP1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TULP1
(R419Q +1 more)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+1 more
GConflicting classifications of pathogenicity
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