List of variants in gene TH reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000360.4(TH):c.241G>A (p.Val81Met)	rs6356	0.31555
NM_000360.4(TH):c.645-74A>T	rs73403741	0.01330
NM_000360.4(TH):c.684G>A (p.Glu228=)	rs11564716	0.00706
NM_000360.4(TH):c.267G>A (p.Arg89=)	rs76240471	0.00521
NM_000360.4(TH):c.579C>T (p.Gly193=)	rs147852210	0.00494
NM_000360.4(TH):c.644+80A>G	rs188105919	0.00449
NM_000360.4(TH):c.695+39G>A	rs73403740	0.00277
NM_000360.4(TH):c.1105-48G>A	rs371445115	0.00076
NM_000360.4(TH):c.372G>A (p.Gly124=)	rs773806238	0.00014
NM_000360.4(TH):c.1048-109G>A	rs544883336
NM_000360.4(TH):c.1201-75G>A	rs116831738
NM_000360.4(TH):c.91-732C>T	rs75888017

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