List of variants in gene SLC25A13 reported as likely benign for not provided

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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: 26

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HGVS	dbSNP	gnomAD frequency
NM_014251.3(SLC25A13):c.933+211C>G	rs116974768	0.02183
NM_014251.3(SLC25A13):c.1018+31T>C	rs76371700	0.01557
NM_014251.3(SLC25A13):c.1177+155C>T	rs116380669	0.01557
NM_014251.3(SLC25A13):c.16-174G>T	rs76679995	0.01442
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.1178-237T>C	rs59694807	0.01226
NM_014251.3(SLC25A13):c.615+36T>C	rs56773234	0.01220
NM_014251.3(SLC25A13):c.1312-133T>C	rs73708481	0.01127
NM_014251.3(SLC25A13):c.755-235C>G	rs60933269	0.01113
NM_014251.3(SLC25A13):c.934-123T>C	rs76207765	0.01055
NM_014251.3(SLC25A13):c.755-297G>C	rs143566020	0.01046
NM_014251.3(SLC25A13):c.1018+46T>G	rs56210033	0.01042
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.1591+56C>T	rs80231631	0.00771
NM_014251.3(SLC25A13):c.1680C>T (p.Ser560=)	rs150082469	0.00244
NM_014251.3(SLC25A13):c.1434G>T (p.Gly478=)	rs146111714	0.00178
NM_014251.3(SLC25A13):c.1841+11T>C	rs370546671	0.00015
NM_014251.3(SLC25A13):c.723T>G (p.Ala241=)	rs577055233	0.00001
NM_014251.3(SLC25A13):c.679_684del
NM_014251.3(SLC25A13):c.1452+19del	rs749506606
NM_014251.3(SLC25A13):c.212+70A>G	rs73710268
NM_014251.3(SLC25A13):c.615+68A>G	rs143747068
NM_014251.3(SLC25A13):c.70-171G>A	rs73235936
NM_014251.3(SLC25A13):c.848+8G>T	rs761126981

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