List of variants in gene combination LOC123956210, SLC26A4 reported as pathogenic for obsolete rare genetic deafness

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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.2168A>G (p.His723Arg)	rs121908362	0.00004
NM_000441.2(SLC26A4):c.2162C>T (p.Thr721Met)	rs121908363	0.00003
NM_000441.2(SLC26A4):c.2188C>T (p.Gln730Ter)	rs397516428

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