List of variants in gene combination LOC129936510, SLC25A38 reported as uncertain significance for autosomal recessive sideroblastic anemia

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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.11A>G (p.Asn4Ser)	rs61995897	0.00151
NM_017875.4(SLC25A38):c.12C>T (p.Asn4=)	rs142420345	0.00066
NM_017875.4(SLC25A38):c.-15C>A	rs1373209338
NM_017875.4(SLC25A38):c.-39G>C	rs375182491

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