ClinVar Miner

List of variants in gene combination SCO2, TYMP reported as likely benign for Mitochondrial DNA depletion syndrome 1

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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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001953.5(TYMP):c.831G>A (p.Leu277=)	rs8141558	0.03453
NM_005138.3(SCO2):c.-135_-132dup	rs143413019

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