List of variants reported as likely benign for T-cell immunodeficiency, congenital alopecia, and nail dystrophy by Illumina Laboratory Services, Illumina

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001369369.1(FOXN1):c.*13T>A	rs73278527	0.00200
NM_001369369.1(FOXN1):c.1556T>A (p.Leu519Gln)	rs34814444	0.00197
NM_001369369.1(FOXN1):c.*626G>C	rs528836565	0.00146
NM_001369369.1(FOXN1):c.1757G>A (p.Cys586Tyr)	rs73278523	0.00128
NM_001369369.1(FOXN1):c.1443G>T (p.Leu481=)	rs548817079

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