RS104894562 FOXN1
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What This Variant Does
"[OMIM:?]
Associated Conditions
T-cell immunodeficiency
congenital alopecia
and nail dystrophy
T-cell lymphopenia
infantile
with or without nail dystrophy
autosomal dominant
Severe combined immunodeficiency disease
T-cell immunodeficiency
congenital alopecia
and nail dystrophy
T-cell lymphopenia
infantile
with or without nail dystrophy
autosomal dominant
Other Variants in FOXN1