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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXN1
(G183R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
FOXN1
(P242S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
FOXN1
(Y455fs)
Deletion
(frameshift variant)
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
GLikely pathogenic
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