List of variants in gene combination LOC130009747, SUCLA2 reported as benign for Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003850.3(SUCLA2):c.90+24G>A	rs9567972	0.71769
NM_003850.3(SUCLA2):c.45C>T (p.Thr15=)	rs35899901	0.00624
NM_003850.3(SUCLA2):c.37G>A (p.Val13Met)	rs35201084	0.00371
NM_003850.3(SUCLA2):c.88C>G (p.Gln30Glu)	rs568437392	0.00001

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