List of variants in gene SLC9A6 reported as likely benign by GeneDx

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: 49

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HGVS	dbSNP	gnomAD frequency
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.170-197A>G	rs180893504	0.00552
NM_001379110.1(SLC9A6):c.885+179G>A	rs782297881	0.00293
NM_001379110.1(SLC9A6):c.1460+6T>C	rs781963949	0.00047
NM_001379110.1(SLC9A6):c.852A>T (p.Ala284=)	rs371472909	0.00015
NM_001379110.1(SLC9A6):c.*12C>T	rs190788663	0.00010
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.1287A>G (p.Gln429=)	rs142161862	0.00006
NM_001379110.1(SLC9A6):c.228T>C (p.Asn76=)	rs782529317	0.00006
NM_001379110.1(SLC9A6):c.-4A>G	rs782090744	0.00004
NM_001379110.1(SLC9A6):c.1434T>C (p.Thr478=)	rs1057520374	0.00004
NM_001379110.1(SLC9A6):c.2021C>T (p.Thr674Met)	rs886044780	0.00004
NM_001379110.1(SLC9A6):c.1307-12G>C	rs372153079	0.00003
NM_001379110.1(SLC9A6):c.170-16T>A	rs548206389	0.00003
NM_001379110.1(SLC9A6):c.564G>A (p.Thr188=)	rs782216766	0.00003
NM_001379110.1(SLC9A6):c.-56-25C>G	rs782396686	0.00002
NM_001379110.1(SLC9A6):c.1143G>A (p.Leu381=)	rs782501407	0.00002
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.516C>T (p.Phe172=)	rs1423014570	0.00002
NM_001379110.1(SLC9A6):c.*16C>G	rs1057522565	0.00001
NM_001379110.1(SLC9A6):c.1038G>T (p.Thr346=)	rs782783023	0.00001
NM_001379110.1(SLC9A6):c.1380C>T (p.Ser460=)	rs782177396	0.00001
NM_001379110.1(SLC9A6):c.1581+10C>T	rs1034902692	0.00001
NM_001379110.1(SLC9A6):c.452A>T (p.His151Leu)	rs796053275	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.638-5A>G	rs1057520615	0.00001
NM_001379110.1(SLC9A6):c.5_8delinsTT	rs797044655
NM_001379110.1(SLC9A6):c.*7T>C	rs2148217238
NM_001379110.1(SLC9A6):c.1006T>C (p.Leu336=)	rs1556618895
NM_001379110.1(SLC9A6):c.1038G>A (p.Thr346=)	rs782783023
NM_001379110.1(SLC9A6):c.1080+80dup	rs35492327
NM_001379110.1(SLC9A6):c.1195-4T>G	rs1057522798
NM_001379110.1(SLC9A6):c.1307-298A>G	rs144085373
NM_001379110.1(SLC9A6):c.1460+14A>G	rs1057520998
NM_001379110.1(SLC9A6):c.1671G>A (p.Lys557=)	rs1556622336
NM_001379110.1(SLC9A6):c.169+14C>G	rs1556614871
NM_001379110.1(SLC9A6):c.370G>A (p.Val124Ile)	rs1556616820
NM_001379110.1(SLC9A6):c.42C>T (p.Ser14=)	rs1057523594
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.900C>T (p.Thr300=)	rs1057520676

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