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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DLAT
(E19Q +1 more)
Single nucleotide variant
(missense variant +2 more)
DLAT-related condition
+3 more
GBenign
DLAT
(Q209R +4 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+1 more
GBenign
DLAT
Deletion
(splice acceptor variant)
not specified
+1 more
GConflicting classifications of pathogenicity
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