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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NLGN4X
Single nucleotide variant
(intron variant)
Asperger syndrome, X-linked, susceptibility to, 2
GUncertain significance
NLGN4X
(P63T)
Single nucleotide variant
(missense variant)
Asperger syndrome, X-linked, susceptibility to, 2
+2 more
GUncertain significance
NLGN4X
(R753S)
Single nucleotide variant
(missense variant)
Asperger syndrome, X-linked, susceptibility to, 2
+2 more
GUncertain significance
NLGN4X
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+5 more
GBenign/Likely benign
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