List of variants in gene SLC9A6 reported as likely benign 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001379110.1(SLC9A6):c.-9G>T	rs367724979	0.00008
NM_001379110.1(SLC9A6):c.1734C>T (p.Ile578=)	rs375760367	0.00008
NM_001379110.1(SLC9A6):c.15C>G (p.Ile5Met)	rs782296172	0.00004
NM_001379110.1(SLC9A6):c.-16C>T	rs139299794	0.00003
NM_001379110.1(SLC9A6):c.-56-25C>G	rs782396686	0.00002
NM_001379110.1(SLC9A6):c.516C>T (p.Phe172=)	rs1423014570	0.00002
NM_001379110.1(SLC9A6):c.2001G>A (p.Pro667=)	rs782708610	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.638-5A>G	rs1057520615	0.00001
NM_001379110.1(SLC9A6):c.1768-6A>G	rs1556623179

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