List of variants in gene SLC25A13 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_014251.3(SLC25A13):c.1884C>T (p.Asn628=)	rs35539807	0.02453
NM_014251.3(SLC25A13):c.933+211C>G	rs116974768	0.02183
NM_014251.3(SLC25A13):c.615+68A>G	rs143747068	0.01955
NM_014251.3(SLC25A13):c.*175A>G	rs144877897	0.01558
NM_014251.3(SLC25A13):c.1592-79G>A	rs114859776	0.01266
NM_014251.3(SLC25A13):c.1177+93G>A	rs73403031	0.01251
NM_014251.3(SLC25A13):c.615+36T>C	rs56773234	0.01220
NM_014251.3(SLC25A13):c.1671C>T (p.Thr557=)	rs79886797	0.01204
NM_014251.3(SLC25A13):c.1018+46T>G	rs56210033	0.01084
NM_014251.3(SLC25A13):c.69+36A>G	rs73405031	0.01029
NM_014251.3(SLC25A13):c.15+240A>G	rs114577678	0.01026
NM_014251.3(SLC25A13):c.675G>A (p.Ser225=)	rs78247004	0.00954
NM_014251.3(SLC25A13):c.212+70A>G	rs73710268
NM_014251.3(SLC25A13):c.70-171G>A	rs73235936

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