ClinVar Miner

List of variants in gene TH reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000360.4(TH):c.267G>A (p.Arg89=)	rs76240471	0.00521
NM_000360.4(TH):c.104T>C (p.Ile35Thr)	rs747420332	0.00006

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