Variants in gene SLC26A4 with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_000441.1(SLC26A4):c.-103T>C	rs60284988	0.00209
NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)	rs111033212	0.00077
NM_000441.2(SLC26A4):c.1246A>C (p.Thr416Pro)	rs28939086	0.00021
NM_000441.2(SLC26A4):c.349C>T (p.Leu117Phe)	rs145254330	0.00017
NM_000441.2(SLC26A4):c.2015G>A (p.Gly672Glu)	rs111033309	0.00009
NM_000441.2(SLC26A4):c.1454C>T (p.Thr485Met)	rs370029782	0.00006
NM_000441.2(SLC26A4):c.1708G>A (p.Val570Ile)	rs397516421	0.00006
NM_000441.2(SLC26A4):c.706C>G (p.Leu236Val)	rs111033242	0.00005
NM_000441.2(SLC26A4):c.1673A>G (p.Asn558Ser)	rs766206507	0.00004
NM_000441.2(SLC26A4):c.1983C>A (p.Asp661Glu)	rs199588131	0.00002
NM_000441.2(SLC26A4):c.397T>C (p.Ser133Pro)	rs121908365	0.00001
NM_000441.2(SLC26A4):c.845G>A (p.Cys282Tyr)	rs111033454	0.00001
NM_000441.2(SLC26A4):c.918+2T>C	rs912147281	0.00001
NM_000441.2(SLC26A4):c.1204G>A (p.Val402Met)	rs397516414
NM_000441.2(SLC26A4):c.716T>A (p.Val239Asp)	rs111033256

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