List of variants in gene SLC9A6 reported as pathogenic by Labcorp Genetics (formerly Invitae), Labcorp

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: 17

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HGVS	dbSNP	gnomAD frequency
NC_000023.10:g.(?_135067662)_(135126883_?)del
NC_000023.10:g.(?_135104725)_(135104876_?)del
NC_000023.10:g.(?_135104725)_(135106662_?)del
NC_000023.10:g.(?_135104735)_(135106652_?)del
NC_000023.10:g.(?_135112271)_(135112341_?)del
NM_001379110.1(SLC9A6):c.1186G>T (p.Gly396Ter)
NM_001379110.1(SLC9A6):c.1246_1249del (p.Leu416fs)	rs2071147098
NM_001379110.1(SLC9A6):c.1418_1419del (p.Phe473fs)
NM_001379110.1(SLC9A6):c.1644del (p.Trp548fs)	rs2148201789
NM_001379110.1(SLC9A6):c.1684dup (p.His562fs)	rs2521459845
NM_001379110.1(SLC9A6):c.370-9_370-5del	rs796053290
NM_001379110.1(SLC9A6):c.445del (p.Arg149fs)	rs2521178978
NM_001379110.1(SLC9A6):c.743+1G>A	rs1556617455
NM_001379110.1(SLC9A6):c.743+3_743+6del	rs2148156632
NM_001379110.1(SLC9A6):c.806dup (p.Lys270fs)	rs2148169894
NM_001379110.1(SLC9A6):c.953G>A (p.Trp318Ter)	rs2148173968
NM_001379110.1(SLC9A6):c.980G>A (p.Trp327Ter)	rs2521310108

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