List of variants in gene combination LIAS, LOC112939935 reported as likely benign for Lipoic acid synthetase deficiency

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

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006859.4(LIAS):c.31A>T (p.Thr11Ser)	rs147516123	0.00014
NM_006859.4(LIAS):c.27C>A (p.Ala9=)	rs553110956	0.00004
NM_006859.4(LIAS):c.18G>A (p.Gly6=)	rs774040503	0.00001
NM_006859.4(LIAS):c.24A>G (p.Ala8=)	rs750426614	0.00001
NM_006859.4(LIAS):c.7C>T (p.Leu3=)	rs1553933562

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