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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ELOVL4
(P273H)
Single nucleotide variant
(missense variant)
Retinal dystrophy
GUncertain significance
ELOVL4
(I267T)
Single nucleotide variant
(missense variant)
Stargardt disease 3
+2 more
GBenign
ELOVL4
(Y199C)
Single nucleotide variant
(missense variant)
Retinal dystrophy
GUncertain significance
ELOVL4
(A18V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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