List of variants in gene TH reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000360.4(TH):c.627C>G (p.Ile209Met)	rs202149985	0.00031
NM_000360.4(TH):c.1277C>T (p.Thr426Met)	rs201330304	0.00003
NM_000360.4(TH):c.52G>A (p.Val18Met)	rs776878220	0.00003
NM_000360.4(TH):c.1430G>C (p.Arg477Pro)
NM_000360.4(TH):c.284C>G (p.Ala95Gly)	rs769126179
NM_000360.4(TH):c.81G>T (p.Glu27Asp)	rs139742336

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