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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NDST1
(R130C)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 46
GUncertain significance
NDST1
(R130H)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 46
GUncertain significance
NDST1
(R244C)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
NDST1
(V295M)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 46
+1 more
GUncertain significance
NDST1
(G823A +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 46
GUncertain significance
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