Variants in gene SLC9A6 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001379110.1(SLC9A6):c.1306+8G>A	rs6654310	0.05510
NM_001379110.1(SLC9A6):c.1689C>T (p.Ser563=)	rs2307131	0.02758
NM_001379110.1(SLC9A6):c.1662-4G>A	rs188072063	0.00703
NM_001379110.1(SLC9A6):c.474T>C (p.Ser158=)	rs144316388	0.00662
NM_001379110.1(SLC9A6):c.1460+4A>G	rs180727016	0.00239
NM_001379110.1(SLC9A6):c.1637G>A (p.Arg546Gln)	rs146263125	0.00166
NM_001379110.1(SLC9A6):c.1460+6T>C	rs781963949	0.00047
NM_001379110.1(SLC9A6):c.1083G>A (p.Leu361=)	rs151178361	0.00022
NM_001379110.1(SLC9A6):c.2001G>A (p.Pro667=)	rs782708610	0.00001
NM_001379110.1(SLC9A6):c.5_8delinsTT	rs797044655
NM_001379110.1(SLC9A6):c.1582-3C>T	rs563279759

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