List of variants in gene FOXI1 reported as benign for nonsyndromic genetic hearing loss

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_012188.5(FOXI1):c.1044T>C (p.Tyr348=)	rs10063424	0.90200
NM_012188.5(FOXI1):c.*440G>A	rs6555887	0.89035
NM_012188.5(FOXI1):c.*535A>G	rs6555888	0.81574
NM_012188.5(FOXI1):c.279G>A (p.Arg93=)	rs2277944	0.29024
NM_012188.5(FOXI1):c.1014G>A (p.Ala338=)	rs55685928	0.00841
NM_012188.5(FOXI1):c.*119C>A	rs6873124

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