List of variants in gene SLC25A38 reported as benign by GeneDx

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_017875.4(SLC25A38):c.793-89A>G	rs9877539	0.92107
NM_017875.4(SLC25A38):c.456+36G>A	rs1995236	0.88451
NM_017875.4(SLC25A38):c.276+249C>T	rs2276715	0.40388
NM_017875.4(SLC25A38):c.165G>A (p.Leu55=)	rs2270770	0.39870
NM_017875.4(SLC25A38):c.626-36G>C	rs870843	0.27843
NM_017875.4(SLC25A38):c.792+171T>A	rs67035835	0.26765
NM_017875.4(SLC25A38):c.*310A>T	rs12991	0.26507
NM_017875.4(SLC25A38):c.792+160A>C	rs35616367	0.26441
NM_017875.4(SLC25A38):c.792+240T>C	rs67353739	0.26434
NM_017875.4(SLC25A38):c.625+291G>A	rs35283414	0.26255
NM_017875.4(SLC25A38):c.793-174T>A	rs35086961	0.25357
NM_017875.4(SLC25A38):c.*588T>A	rs6890	0.12968
NM_017875.4(SLC25A38):c.793-224C>T	rs11712093	0.12666
NM_017875.4(SLC25A38):c.793-175A>T	rs73058289	0.11485
NM_017875.4(SLC25A38):c.70-192A>G	rs6803881	0.04965
NM_017875.4(SLC25A38):c.792+293C>G	rs6793498	0.04057
NM_017875.4(SLC25A38):c.69+257C>T	rs111624230	0.02305
NM_017875.4(SLC25A38):c.625+71A>G	rs72867422	0.02176
NM_017875.4(SLC25A38):c.792+98A>C	rs78965445	0.02109
NM_017875.4(SLC25A38):c.*472G>T	rs141567816	0.01562
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.*212T>G	rs72867427
NM_017875.4(SLC25A38):c.277-147C>T	rs45503293
NM_017875.4(SLC25A38):c.625+241T>C	rs13081742
NM_017875.4(SLC25A38):c.793-175dup	rs34894781

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