List of variants in gene ATRX reported as pathogenic for hematologic disorder

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_000489.6(ATRX):c.109C>T (p.Arg37Ter)	rs122445108
NM_000489.6(ATRX):c.236C>G (p.Ser79Ter)	rs122445107
NM_000489.6(ATRX):c.736C>T (p.Arg246Cys)	rs122445105

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