List of variants in gene SLC25A38 reported as likely benign for hematologic disorder

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_017875.4(SLC25A38):c.*588T>A	rs6890	0.12968
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.-209A>G	rs143903497	0.01332
NM_017875.4(SLC25A38):c.-292G>A	rs142441701	0.01159
NM_017875.4(SLC25A38):c.*809C>T	rs71325527	0.00540
NM_017875.4(SLC25A38):c.239C>G (p.Thr80Arg)	rs144149294	0.00385
NM_017875.4(SLC25A38):c.196A>G (p.Arg66Gly)	rs34127778	0.00344
NM_017875.4(SLC25A38):c.382A>G (p.Met128Val)	rs146940902	0.00282
NM_017875.4(SLC25A38):c.*304C>T	rs113251543	0.00262
NM_017875.4(SLC25A38):c.*490G>A	rs150889211	0.00096
NM_017875.4(SLC25A38):c.*549G>A	rs189387075	0.00023
NM_017875.4(SLC25A38):c.-273G>A	rs184769974

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