List of variants in gene SLC9A6 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 6

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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	0.03011
NM_001379110.1(SLC9A6):c.1551-98T>G	rs2279595	0.02267
NM_001379110.1(SLC9A6):c.170-125C>T	rs138795073	0.01102
NM_001379110.1(SLC9A6):c.1637G>A (p.Arg546Gln)	rs146263125	0.00166
NM_001379110.1(SLC9A6):c.1081-8C>T	rs1060504684	0.00001

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