ClinVar Miner

List of variants in gene FOXI1 reported as likely benign for Autosomal recessive nonsyndromic hearing loss 4; Pendred syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012188.5(FOXI1):c.231C>G (p.Pro77=)	rs550209761	0.00051
NM_012188.5(FOXI1):c.823G>A (p.Ala275Thr)	rs145129881	0.00021

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