List of variants in gene ARX studied for See cases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 Xp21.3(chrX:25025253-25025855)x2
GRCh37/hg19 Xp21.3(chrX:25025725-25025855)x3
NM_139058.3(ARX):c.30C>A (p.Cys10Ter)	rs794726959
NM_139058.3(ARX):c.596C>G (p.Thr199Arg)	rs1268774120
NM_139058.3(ARX):c.96C>G (p.Ile32Met)

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