List of variants in gene FOXI1 reported as uncertain significance 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)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_012188.5(FOXI1):c.1088G>T (p.Ser363Ile)	rs150705492	0.00031
NM_012188.5(FOXI1):c.1090G>A (p.Val364Ile)	rs201090454	0.00022
NM_012188.5(FOXI1):c.1013C>T (p.Ala338Val)	rs367809742	0.00020
NM_012188.5(FOXI1):c.773G>A (p.Gly258Glu)	rs121909340	0.00005
NM_012188.5(FOXI1):c.545A>G (p.Lys182Arg)	rs772882906	0.00003
NM_012188.5(FOXI1):c.937G>C (p.Gly313Arg)	rs755810719	0.00002
NM_012188.5(FOXI1):c.-18G>A	rs764490860	0.00001
NM_012188.5(FOXI1):c.763G>A (p.Ala255Thr)	rs951259617	0.00001
NM_012188.5(FOXI1):c.307G>T (p.Gly103Trp)	rs1053809070

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