ClinVar for MedGen (Select 101814) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 827575	NM_001369369.1(FOXN1):c.1089_1103del (p.Trp363_Pro368delinsCys)	FOXN1	Deletion (inframe_indel)	T-lymphocyte deficiency +1 more	GPathogenic
Select item 827574	NM_001369369.1(FOXN1):c.933_936dup (p.Asp313fs)	FOXN1 (D313fs)	Duplication (frameshift variant)	T-cell immunodeficiency, congenital alopecia, and nail dystrophy	GPathogenic FDA Recognized database