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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LINS1
(V448G +2 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal recessive 27
GUncertain significance
LINS1
Single nucleotide variant
(splice donor variant)
Intellectual disability, autosomal recessive 27
GLikely pathogenic
LINS1
(I173V +1 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual disability, autosomal recessive 27
GUncertain significance
LINS1
(H111P)
Single nucleotide variant
(missense variant +2 more)
Intellectual disability, autosomal recessive 27
GUncertain significance
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