"Ambry Genetics"[submitter] AND "SLC26A4-AS1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2221861	NM_000441.2(SLC26A4):c.104A>T (p.Gln35Leu)	SLC26A4, SLC26A4-AS1 (Q35L)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2277403	NM_000441.2(SLC26A4):c.128G>T (p.Arg43Leu)	SLC26A4, SLC26A4-AS1 (R43L)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance