List of variants in gene combination LOC123956210, SLC26A4 reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 4

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Gene type: Distinguish antisense genes from sense genes
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.2119G>A (p.Gly707Arg)	rs372072732	0.00004
NM_000441.2(SLC26A4):c.2131G>A (p.Asp711Asn)	rs145805875
NM_000441.2(SLC26A4):c.2135A>G (p.Asn712Ser)	rs772522003

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