List of variants in gene SLC9A6 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001379110.1(SLC9A6):c.1385C>T (p.Thr462Met)	rs1229345478	0.00001
NM_001379110.1(SLC9A6):c.256A>G (p.Ser86Gly)	rs587784401	0.00001
NM_001379110.1(SLC9A6):c.*1G>C	rs2521487076
NM_001379110.1(SLC9A6):c.*4T>C	rs2521487124
NM_001379110.1(SLC9A6):c.178G>A (p.Val60Met)	rs906567942
NM_001379110.1(SLC9A6):c.529A>G (p.Ile177Val)	rs587784402

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