Variants in gene SLC26A4 with conflicting interpretations "affects" and "pathogenic"

Submission 1 (affects) minimum review status:		Submission 1 (affects) 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: 28

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HGVS	dbSNP	gnomAD frequency
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.1334T>G (p.Leu445Trp)	rs111033307	0.00008
NM_000441.2(SLC26A4):c.1226G>A (p.Arg409His)	rs111033305	0.00006
NM_000441.2(SLC26A4):c.1489G>A (p.Gly497Ser)	rs111033308	0.00006
NM_000441.2(SLC26A4):c.1229C>T (p.Thr410Met)	rs111033220	0.00004
NM_000441.2(SLC26A4):c.1667A>G (p.Tyr556Cys)	rs763006761	0.00002
NM_000441.2(SLC26A4):c.1694G>A (p.Cys565Tyr)	rs111033257	0.00001
NM_000441.2(SLC26A4):c.1707+5G>A	rs192366176	0.00001
NM_000441.2(SLC26A4):c.1975G>C (p.Val659Leu)	rs200455203	0.00001
NM_000441.2(SLC26A4):c.2007C>A (p.Asp669Glu)	rs749013429	0.00001
NM_000441.2(SLC26A4):c.2048T>C (p.Phe683Ser)	rs1060499808	0.00001
NM_000441.2(SLC26A4):c.439A>G (p.Met147Val)	rs760413427	0.00001
NM_000441.2(SLC26A4):c.578C>T (p.Thr193Ile)	rs111033348	0.00001
NM_000441.2(SLC26A4):c.1001G>T (p.Gly334Val)	rs146281367
NM_000441.2(SLC26A4):c.1105A>G (p.Lys369Glu)	rs121908361
NM_000441.2(SLC26A4):c.1115C>T (p.Ala372Val)	rs121908364
NM_000441.2(SLC26A4):c.1174A>T (p.Asn392Tyr)	rs201562855
NM_000441.2(SLC26A4):c.1262A>T (p.Gln421Leu)	rs201660407
NM_000441.2(SLC26A4):c.1371C>A (p.Asn457Lys)	rs1554359670
NM_000441.2(SLC26A4):c.1579A>C (p.Thr527Pro)	rs1554360358
NM_000441.2(SLC26A4):c.1586T>G (p.Ile529Ser)	rs786204739
NM_000441.2(SLC26A4):c.2074T>C (p.Phe692Leu)	rs1399914687
NM_000441.2(SLC26A4):c.226C>T (p.Pro76Ser)	rs1554352676
NM_000441.2(SLC26A4):c.296C>G (p.Thr99Arg)	rs141142414
NM_000441.2(SLC26A4):c.601-1G>A	rs1554355011
NM_000441.2(SLC26A4):c.716T>A (p.Val239Asp)	rs111033256
NM_000441.2(SLC26A4):c.82A>G (p.Ser28Gly)	rs1554352234

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