List of variants in gene SLC9A6 reported as benign by Genetic Services Laboratory, University of Chicago

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: 8

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HGVS	dbSNP	gnomAD frequency
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.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.1582-3C>T	rs563279759	0.00017

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