List of variants in gene combination LOC129998833, SLC25A13 reported as likely benign for inborn disorder of amino acid metabolism

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_014251.3(SLC25A13):c.6G>T (p.Ala2=)	rs774562949	0.00007
NM_014251.3(SLC25A13):c.12C>T (p.Ala4=)	rs961482670	0.00001
NM_014251.3(SLC25A13):c.15+15G>C
NM_014251.3(SLC25A13):c.15+7G>A
NM_014251.3(SLC25A13):c.15+8C>T
NM_014251.3(SLC25A13):c.15+9G>A	rs1044447024
NM_014251.3(SLC25A13):c.9C>T (p.Ala3=)	rs771172427

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