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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DOCK8, LOC126860552
(P105R +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
DOCK8
(I126M +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive hyper-IgE syndrome
+2 more
GConflicting classifications of pathogenicity
DOCK8
(A229P +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
DOCK8
(E917K +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
DOCK8
(T1088M +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
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