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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRNT1
(R203K)
Single nucleotide variant
(missense variant +1 more)
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
GLikely pathogenic
ARL8B, BHLHE40
+12 more
Copy number loss
Seizure
+2 more
GLikely pathogenic