List of variants in gene ATRX reported as likely benign for Acquired hemoglobin H disease; Alpha thalassemia-X-linked intellectual disability syndrome; Intellectual disability-hypotonic facies syndrome, X-linked, 1

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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.228G>A (p.Ser76=)	rs5959371	0.03016
NM_000489.6(ATRX):c.2169G>C (p.Glu723Asp)	rs61752456	0.00041
NM_000489.6(ATRX):c.570T>G (p.Pro190=)	rs188831993	0.00009

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