ClinVar Miner

List of variants in gene WHRN reported as likely pathogenic for Autosomal recessive nonsyndromic hearing loss 31

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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_015404.4(WHRN):c.1943C>A (p.Ser648Tyr)	rs142653982	0.00098
NM_015404.4(WHRN):c.2644C>A (p.Arg882Ser)	rs150586098

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