List of variants in gene combination LOC130067864, TYMP reported as uncertain significance for mitochondrial DNA depletion syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001953.5(TYMP):c.242G>A (p.Arg81Gln)	rs143789597	0.00135
NM_001953.5(TYMP):c.228G>A (p.Met76Ile)	rs1064792859

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