List of variants in gene SLC26A4 reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.707T>C (p.Leu236Pro)	rs80338848	0.00035
NM_000441.2(SLC26A4):c.1001+1G>A	rs80338849	0.00029
NM_000441.2(SLC26A4):c.1246A>C (p.Thr416Pro)	rs28939086	0.00021
NM_000441.2(SLC26A4):c.919-2A>G	rs111033313	0.00018
NM_000441.2(SLC26A4):c.1151A>G (p.Glu384Gly)	rs111033244	0.00016
NM_000441.2(SLC26A4):c.2015G>A (p.Gly672Glu)	rs111033309	0.00009
NM_000441.2(SLC26A4):c.1223C>T (p.Ser408Phe)	rs1584325160
NM_000441.2(SLC26A4):c.1540C>A (p.Gln514Lys)	rs121908366
NM_000441.2(SLC26A4):c.2317G>A (p.Glu773Lys)	rs764791809
NM_000441.2(SLC26A4):c.716T>A (p.Val239Asp)	rs111033256

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