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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LONP1
(H742Y +2 more)
Single nucleotide variant
(missense variant +1 more)
CODAS syndrome
GUncertain significance
LONP1
(V466G +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
LONP1
(A542V +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
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