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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ITGB2
(G637R +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency 1
+1 more
GUncertain significance
ITGB2
(G399S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ITGB2
(R448Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ITGB2
(V370A +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ITGB2
(A321T +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency 1
+1 more
GUncertain significance
ITGB2
(R285C +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
ITGB2
(N146D +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ITGB2
(K209Q +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency 1
+1 more
GUncertain significance
ITGB2
(F99S +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency 1
+1 more
GUncertain significance
ITGB2
(A85T +1 more)
Single nucleotide variant
(missense variant)
Leukocyte adhesion deficiency 1
+2 more
GUncertain significance
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