List of variants in gene SLC25A15 reported as likely benign by Illumina Laboratory Services, Illumina

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_014252.4(SLC25A15):c.-67A>T	rs112276566	0.00623
NM_014252.4(SLC25A15):c.*58G>T	rs17090557	0.00553
NM_014252.4(SLC25A15):c.182G>A (p.Arg61His)	rs34615430	0.00292
NM_014252.4(SLC25A15):c.*606C>G	rs555003166	0.00174
NM_014252.4(SLC25A15):c.*1829AAAAG[2]	rs201178711
NM_014252.4(SLC25A15):c.*2438G>A	rs181523869

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