List of variants in gene SLC26A6 reported as uncertain significance by Martin Pollak Laboratory, Beth Israel Deaconess Medical Center

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_022911.3(SLC26A6):c.1566G>A (p.Thr522=)	rs387907501	0.00001
NM_022911.3(SLC26A6):c.1631G>A (p.Arg544His)	rs387907495	0.00001
NM_022911.3(SLC26A6):c.1541C>T (p.Ser514Phe)	rs387907499
NM_022911.3(SLC26A6):c.1618G>C (p.Val540Leu)	rs387907494
NM_022911.3(SLC26A6):c.1653T>A (p.Phe551Leu)	rs387907502
NM_022911.3(SLC26A6):c.1902C>T (p.Ser634=)	rs387907493
NM_022911.3(SLC26A6):c.2081A>T (p.His694Leu)	rs387907500
NM_022911.3(SLC26A6):c.365G>A (p.Gly122Asp)	rs387907497
NM_022911.3(SLC26A6):c.682G>C (p.Val228Leu)	rs387907498
NM_022911.3(SLC26A6):c.709C>A (p.Leu237Ile)	rs387907496

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