ClinVar Miner

List of variants in gene combination LOC130067862, TYMP reported as likely benign for Mitochondrial neurogastrointestinal encephalomyopathy

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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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001953.5(TYMP):c.910G>A (p.Asp304Asn)	rs570438867

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