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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TECR
(P54R +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 14
GUncertain significance
TECR
(V88L +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance