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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRBA
(F2763L +3 more)
Single nucleotide variant
(missense variant)
Combined immunodeficiency due to LRBA deficiency
GUncertain significance
MAB21L2, LRBA
(R51G)
Single nucleotide variant
(missense variant +1 more)
Colobomatous microphthalmia-rhizomelic dysplasia syndrome
GPathogenic
LRBA
(R1445*)
Single nucleotide variant
(nonsense)
Severe combined immunodeficiency due to CORO1A deficiency
GPathogenic
LRBA
Single nucleotide variant
(splice acceptor variant)
Combined immunodeficiency due to LRBA deficiency
+1 more
GLikely pathogenic
LRBA
(H288fs)
Deletion
(frameshift variant)
Combined immunodeficiency due to LRBA deficiency
GLikely pathogenic
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