List of variants in gene SLC25A38 reported as uncertain significance for Refractory anemia with ringed sideroblasts

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_017875.4(SLC25A38):c.*431G>A	rs73058292	0.00540
NM_017875.4(SLC25A38):c.-161G>A	rs528990278	0.00120
NM_017875.4(SLC25A38):c.*404G>A	rs886058473	0.00011
NM_017875.4(SLC25A38):c.*370C>T	rs886058472	0.00004
NM_017875.4(SLC25A38):c.288A>G (p.Arg96=)	rs765578993	0.00001
NM_017875.4(SLC25A38):c.652A>T (p.Ile218Phe)	rs764125735	0.00001
NM_017875.4(SLC25A38):c.570C>A (p.Pro190=)	rs886058471

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