List of variants in gene FOXN1 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001369369.1(FOXN1):c.546C>T (p.Asn182=)	rs62640040	0.00125
NM_001369369.1(FOXN1):c.1618G>A (p.Asp540Asn)	rs181483148	0.00013
NM_001369369.1(FOXN1):c.988G>A (p.Glu330Lys)	rs199983506	0.00009
NM_001369369.1(FOXN1):c.411G>A (p.Glu137=)	rs760960446	0.00002
NM_001369369.1(FOXN1):c.1855G>C (p.Ala619Pro)	rs141857607	0.00001
NM_001369369.1(FOXN1):c.1075G>A (p.Glu359Lys)	rs2069998681
NM_001369369.1(FOXN1):c.1178del (p.Gly393fs)
NM_001369369.1(FOXN1):c.1201_1216del (p.Pro401fs)	rs1064793129
NM_001369369.1(FOXN1):c.1313C>A (p.Pro438His)	rs2070016524
NM_001369369.1(FOXN1):c.1318C>T (p.Gln440Ter)
NM_001369369.1(FOXN1):c.1799C>T (p.Pro600Leu)
NM_001369369.1(FOXN1):c.668T>G (p.Met223Arg)
NM_001369369.1(FOXN1):c.830+1G>T	rs1567882296

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