List of variants in gene SLC9A1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003047.5(SLC9A1):c.226C>T (p.His76Tyr)	rs141715004	0.00084
NM_003047.5(SLC9A1):c.2275G>A (p.Asp759Asn)	rs140504210	0.00028
NM_003047.5(SLC9A1):c.176A>T (p.Asp59Val)	rs761485124	0.00003

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