List of variants in gene ARX reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_139058.3(ARX):c.1610T>C (p.Leu537Pro)	rs1189193466
NM_139058.3(ARX):c.596C>A (p.Thr199Lys)	rs1268774120
NM_139058.3(ARX):c.611G>C (p.Arg204Pro)	rs755745002
NM_139058.3(ARX):c.90C>G (p.Asp30Glu)	rs2147325437

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