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

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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_012188.5(FOXI1):c.*924C>T	rs45466695	0.05560
NM_012188.5(FOXI1):c.*331G>C	rs72828668	0.01897
NM_012188.5(FOXI1):c.*556A>G	rs77823283	0.01117
NM_012188.5(FOXI1):c.*143A>T	rs55762796

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