List of variants in gene SLC26A2 reported as likely benign by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000112.4(SLC26A2):c.*2617C>T	rs188922059	0.01558
NM_000112.4(SLC26A2):c.*4391G>T	rs150508217	0.01531
NM_000112.4(SLC26A2):c.*3466C>G	rs6888879	0.01309
NM_000112.4(SLC26A2):c.*2612C>T	rs28451300	0.01303
NM_000112.4(SLC26A2):c.*4799G>A	rs72832119	0.01211
NM_000112.4(SLC26A2):c.*4930C>T	rs79521091	0.00981
NM_000112.4(SLC26A2):c.*83T>G	rs143847430	0.00356
NM_000112.4(SLC26A2):c.987T>C (p.Leu329=)	rs116302615	0.00246
NM_000112.4(SLC26A2):c.2087A>G (p.Asn696Ser)	rs34351171	0.00214
NM_000112.4(SLC26A2):c.468C>T (p.Thr156=)	rs111788154	0.00110
NM_000112.4(SLC26A2):c.699+20T>C	rs368382498	0.00022
NM_000112.4(SLC26A2):c.807C>T (p.Ala269=)	rs148445106	0.00014
NM_000112.4(SLC26A2):c.1194A>T (p.Val398=)	rs886038240	0.00005

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