List of variants in gene SLC9A6 reported as pathogenic by ClinGen Rett and Angelman-like Disorders Variant Curation Expert Panel

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_001379110.1(SLC9A6):c.370-9_370-5del	rs796053290
NM_001379110.1(SLC9A6):c.448-1G>A	rs797044508
NM_001379110.1(SLC9A6):c.916C>T (p.Gln306Ter)	rs398124224

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