U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Search results

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXN1
(E159K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
FOXN1
(I278V)
Single nucleotide variant
(missense variant)
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
+3 more
GUncertain significance
FOXN1
(A619P)
Single nucleotide variant
(missense variant)
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
+1 more
GUncertain significance
Format
Sort by
Choose Destination