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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLA2G6
(R656H +4 more)
Single nucleotide variant
(missense variant)
Infantile neuroaxonal dystrophy
+3 more
GConflicting classifications of pathogenicity
PLA2G6
(E493G +4 more)
Single nucleotide variant
(missense variant)
Infantile neuroaxonal dystrophy
+1 more
GLikely pathogenic