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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EIF2B2
(G200V)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic
EIF2B2, MLH3
Single nucleotide variant
(3 prime UTR variant)
Vanishing white matter disease
+2 more
GLikely benign