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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NDST1
(R454C)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 46
+1 more
GUncertain significance
NDST1
(T801S +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 46
GUncertain significance