List of variants in gene SLC9A6 reported as likely benign for not provided

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: 48

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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_006359.2(SLC9A6):c.-349C>T	rs138591582	0.01486
NM_001379110.1(SLC9A6):c.170-125C>T	rs138795073	0.01102
NM_001379110.1(SLC9A6):c.1768-219A>G	rs147850191	0.00758
NM_001379110.1(SLC9A6):c.1662-4G>A	rs188072063	0.00707
NM_001379110.1(SLC9A6):c.170-197A>G	rs180893504	0.00552
NM_001379110.1(SLC9A6):c.448-5G>T	rs372580592	0.00549
NM_001379110.1(SLC9A6):c.885+179G>A	rs782297881	0.00293
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.1460+6T>C	rs781963949	0.00047
NM_001379110.1(SLC9A6):c.1083G>A (p.Leu361=)	rs151178361	0.00022
NM_001379110.1(SLC9A6):c.1582-3C>T	rs563279759	0.00017
NM_001379110.1(SLC9A6):c.852A>T (p.Ala284=)	rs371472909	0.00015
NM_001379110.1(SLC9A6):c.-9G>T	rs367724979	0.00008
NM_001379110.1(SLC9A6):c.1551-11T>C	rs147479371	0.00007
NM_001379110.1(SLC9A6):c.524+3A>G	rs372679456	0.00007
NM_001379110.1(SLC9A6):c.1287A>G (p.Gln429=)	rs142161862	0.00006
NM_001379110.1(SLC9A6):c.228T>C (p.Asn76=)	rs782529317	0.00006
NM_001379110.1(SLC9A6):c.15C>G (p.Ile5Met)	rs782296172	0.00004
NM_001379110.1(SLC9A6):c.1307-12G>C	rs372153079	0.00003
NM_001379110.1(SLC9A6):c.564G>A (p.Thr188=)	rs782216766	0.00003
NM_001379110.1(SLC9A6):c.1269G>C (p.Lys423Asn)	rs781918578	0.00002
NM_001379110.1(SLC9A6):c.1581+17G>A	rs917623322	0.00002
NM_001379110.1(SLC9A6):c.1038G>T (p.Thr346=)	rs782783023	0.00001
NM_001379110.1(SLC9A6):c.1081-8C>T	rs1060504684	0.00001
NM_001379110.1(SLC9A6):c.1863G>A (p.Pro621=)	rs782665428	0.00001
NM_001379110.1(SLC9A6):c.517G>A (p.Val173Ile)	rs782117973	0.00001
NM_001379110.1(SLC9A6):c.57C>T (p.Ser19=)	rs781963863	0.00001
NM_001379110.1(SLC9A6):c.744-7T>C	rs1556618483	0.00001
NM_001379110.1(SLC9A6):c.5_8delinsTT	rs797044655
NM_001379110.1(SLC9A6):c.*7T>C	rs2148217238
NM_001379110.1(SLC9A6):c.1080+80dup	rs35492327
NM_001379110.1(SLC9A6):c.1164C>T (p.Val388=)	rs1556619315
NM_001379110.1(SLC9A6):c.1307-298A>G	rs144085373
NM_001379110.1(SLC9A6):c.1389T>C (p.Leu463=)	rs1556620345
NM_001379110.1(SLC9A6):c.1503T>C (p.His501=)	rs2071271908
NM_001379110.1(SLC9A6):c.170-6T>A
NM_001379110.1(SLC9A6):c.1812T>C (p.Asn604=)
NM_001379110.1(SLC9A6):c.1869A>T (p.Thr623=)	rs2071565905
NM_001379110.1(SLC9A6):c.321T>C (p.Ile107=)
NM_001379110.1(SLC9A6):c.487G>A (p.Ala163Thr)	rs796053281
NM_001379110.1(SLC9A6):c.637+206dup	rs1241262472
NM_001379110.1(SLC9A6):c.744-208del	rs376254654
NM_001379110.1(SLC9A6):c.744-48dup	rs200585663
NM_001379110.1(SLC9A6):c.837C>T (p.Phe279=)	rs2521290502

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