C1866426[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 379390	NM_001369369.1(FOXN1):c.124-20G>A	FOXN1	Single nucleotide variant (intron variant)	T-cell immunodeficiency, congenital alopecia, and nail dystrophy +2 more	GBenign
Select item 379409	NM_001369369.1(FOXN1):c.830+19A>G	FOXN1	Single nucleotide variant (intron variant)	T-cell immunodeficiency, congenital alopecia, and nail dystrophy +2 more	GBenign
Select item 322436	NM_001369369.1(FOXN1):c.1795G>C (p.Ala599Pro)	FOXN1 (A599P)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign

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