ClinVar Miner

List of variants in gene SLC26A4 reported as likely pathogenic by Otorhinolaryngology Lab - LIM32, University of Sao Paulo School of Medicine Clinics Hospital

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.1615-2A>G	rs758823761	0.00001
NM_000441.2(SLC26A4):c.481T>A (p.Phe161Ile)	rs1481765326	0.00001

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