List of variants in gene SLC26A4 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.1826T>G (p.Val609Gly)	rs17154335	0.04399
NM_000441.2(SLC26A4):c.1708-18T>A	rs55701254	0.02432
NM_000441.2(SLC26A4):c.2218G>A (p.Gly740Ser)	rs17154353	0.01449
NM_000441.2(SLC26A4):c.1002-9A>C	rs10234822	0.01002
NM_000441.2(SLC26A4):c.1488C>T (p.Leu496=)	rs77407094	0.00782
NM_000441.2(SLC26A4):c.1790T>C (p.Leu597Ser)	rs55638457	0.00545
NM_000441.2(SLC26A4):c.416-13T>C	rs77553387	0.00455
NM_000441.2(SLC26A4):c.849G>C (p.Met283Ile)	rs146348818	0.00293
NM_000441.2(SLC26A4):c.1545-5T>G	rs77944876	0.00234
NM_000441.2(SLC26A4):c.1614+8C>T	rs370184422	0.00032
NM_000441.2(SLC26A4):c.416-16G>T	rs114992866

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