List of variants in gene combination ARX, LOC109610631 reported as likely pathogenic for electroclinical syndrome

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_139058.3(ARX):c.303_323dup (p.Ala109_Ala115dup)	rs2147324381
NM_139058.3(ARX):c.306GGC[17] (p.Ala109_Ala115dup)	rs387906492
NM_139058.3(ARX):c.426_449dup (p.Gly143_Ala150dup)	rs1569395541

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