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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXN1
(C399fs)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
FOXN1
(R482Q)
Single nucleotide variant
(missense variant)
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
+2 more
GUncertain significance