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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ITCH
(G9R)
Single nucleotide variant
(missense variant +1 more)
Syndromic multisystem autoimmune disease due to ITCH deficiency
GUncertain significance
ITCH
Microsatellite
(splice donor variant)
Syndromic multisystem autoimmune disease due to ITCH deficiency
GLikely pathogenic