ClinVar Miner

List of variants in gene SLC25A38 reported as benign for X-linked sideroblastic anemia 1

Included ClinVar conditions (1):

X-linked sideroblastic anemia 1

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_017875.4(SLC25A38):c.*642del	rs34288981

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