ClinVar Miner

List of variants reported as pathogenic for autosomal recessive nonsyndromic hearing loss 4 by UAEU Genomics Laboratory, United Arab Emirates University

Included ClinVar conditions (4):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.1337A>G (p.Gln446Arg)	rs768471577
NM_000441.2(SLC26A4):c.248G>A (p.Trp83Ter)
NM_000441.2(SLC26A4):c.716T>A (p.Val239Asp)	rs111033256

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