List of variants in gene SLC25A13 reported as uncertain significance 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_014251.3(SLC25A13):c.1910T>C (p.Val637Ala)	rs148962110	0.00075
NM_014251.3(SLC25A13):c.1336A>C (p.Thr446Pro)	rs200237622	0.00004
NM_014251.3(SLC25A13):c.1157G>C (p.Gly386Ala)	rs776461118	0.00002
NM_014251.3(SLC25A13):c.1637C>G (p.Thr546Arg)	rs548769905	0.00001
NM_014251.3(SLC25A13):c.874C>T (p.Arg292Trp)	rs142308242	0.00001
NM_014251.3(SLC25A13):c.1201G>A (p.Val401Ile)	rs1243282367
NM_014251.3(SLC25A13):c.70T>C (p.Tyr24His)

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