ClinVar Miner

List of variants reported as not provided for autosomal recessive nonsyndromic hearing loss 4

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.2015G>A (p.Gly672Glu)	rs111033309	0.00010
NM_000441.2(SLC26A4):c.716T>A (p.Val239Asp)	rs111033256	0.00005
NM_000441.2(SLC26A4):c.304G>A (p.Gly102Arg)	rs1219724284

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