List of variants in gene TYMP reported as benign for Mitochondrial neurogastrointestinal encephalomyopathy

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001953.5(TYMP):c.204C>T (p.Gly68=)	rs34375653	0.01755
NM_001953.5(TYMP):c.735G>A (p.Gln245=)	rs139223629	0.00222
NM_001953.5(TYMP):c.194G>A (p.Ser65Asn)	rs570047465

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