List of variants in gene SLC25A13 reported as uncertain significance by Shenzhen Institute of Pediatrics, Shenzhen Children's Hospital

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014251.3(SLC25A13):c.1311C>T (p.Cys437=)	rs879255502	0.00003
NM_014251.3(SLC25A13):c.1958A>G (p.Lys653Arg)	rs879255501	0.00001
NM_014251.3(SLC25A13):c.616-11A>G	rs879255503

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