List of variants in gene TYMP reported as likely benign for hereditary skeletal muscle disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001953.5(TYMP):c.495T>C (p.Asn165=)	rs372889443	0.00005
NM_001953.5(TYMP):c.516+9C>T	rs201884709	0.00005
NM_001953.5(TYMP):c.177C>T (p.Ala59=)	rs137930991	0.00004
NM_001953.5(TYMP):c.198G>A (p.Ala66=)	rs1172184794	0.00001

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