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Items: 33

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NLGN4X
Single nucleotide variant
(synonymous variant)
NLGN4X-related condition
+3 more
GBenign/Likely benign
NLGN4X
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign
NLGN4X
(R753S)
Single nucleotide variant
(missense variant)
Asperger syndrome, X-linked, susceptibility to, 2
+2 more
GUncertain significance
NLGN4X
Single nucleotide variant
(synonymous variant)
NLGN4X-related condition
+1 more
GLikely benign
NLGN4X
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign/Likely benign
NLGN4X
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign/Likely benign
NLGN4X
(L593F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GBenign/Likely benign
NLGN4X
(R583Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NLGN4X
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
NLGN4X
(V522M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NLGN4X
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
NLGN4X
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
NLGN4X
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
NLGN4X
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
NLGN4X
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GBenign
NLGN4X
(L406I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NLGN4X
(V371I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NLGN4X
(V348I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NLGN4X
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
NLGN4X
(K324R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
NLGN4X
(N320S)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
NLGN4X
(T312M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NLGN4X
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GBenign
NLGN4X
Single nucleotide variant
(synonymous variant)
NLGN4X-related condition
+5 more
GBenign/Likely benign
NLGN4X
Single nucleotide variant
(synonymous variant)
NLGN4X-related condition
+1 more
GConflicting classifications of pathogenicity
NLGN4X
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign/Likely benign
NLGN4X
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
NLGN4X
(I159T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NLGN4X
(G84R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NLGN4X
(I39V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
NLGN4X
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
NLGN4X
Single nucleotide variant
(synonymous variant)
NLGN4X-related condition
+1 more
GConflicting classifications of pathogenicity
LOC105373156, NLGN4X
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GBenign
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