List of variants in gene FOXI3 reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001135649.3(FOXI3):c.148G>C (p.Ala50Pro)	rs550296238	0.00409
NM_001135649.3(FOXI3):c.337GCGCCCGCC[3] (p.113APA[3])	rs757327073
NM_001135649.3(FOXI3):c.438G>A (p.Pro146=)
NM_001135649.3(FOXI3):c.483G>T (p.Ala161=)

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