List of variants in gene SLC9A6 reported as benign for not specified

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: 18

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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.744-6C>T	rs17001258	0.01856
NM_001379110.1(SLC9A6):c.1662-4G>A	rs188072063	0.00707
NM_001379110.1(SLC9A6):c.474T>C (p.Ser158=)	rs144316388	0.00625
NM_001379110.1(SLC9A6):c.1029A>C (p.Ala343=)	rs142049079	0.00390
NM_001379110.1(SLC9A6):c.1460+4A>G	rs180727016	0.00236
NM_001379110.1(SLC9A6):c.1637G>A (p.Arg546Gln)	rs146263125	0.00166
NM_001379110.1(SLC9A6):c.*8A>T	rs200171451	0.00157
NM_001379110.1(SLC9A6):c.5_6del	rs781795776	0.00149
NM_001379110.1(SLC9A6):c.1460+10A>G	rs185533973	0.00026
NM_001379110.1(SLC9A6):c.1582-3C>T	rs563279759	0.00017
NM_001379110.1(SLC9A6):c.1581+11G>A	rs375145994	0.00012
NM_001379110.1(SLC9A6):c.-16C>T	rs139299794	0.00003
NM_001379110.1(SLC9A6):c.801G>A (p.Ala267=)	rs185192141	0.00002
NM_001379110.1(SLC9A6):c.5_8delinsTT	rs797044655
NM_001379110.1(SLC9A6):c.448-6del	rs375038684
NM_001379110.1(SLC9A6):c.448-6dup	rs375038684

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