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

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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_017875.4(SLC25A38):c.*472G>T	rs141567816	0.01690
NM_017875.4(SLC25A38):c.-303A>C	rs114422738	0.01335
NM_017875.4(SLC25A38):c.*809C>T	rs71325527	0.00540
NM_017875.4(SLC25A38):c.382A>G (p.Met128Val)	rs146940902	0.00282

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