ClinVar Miner

List of variants in gene TG reported as likely benign by GeneDx

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_003235.5(TG):c.199G>A (p.Gly67Ser)	rs116340633	0.00871
NM_003235.5(TG):c.4527C>T (p.His1509=)	rs201216611	0.00037

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