List of variants in gene TBX20 reported as benign by Ambry Genetics

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_001077653.2(TBX20):c.39T>C (p.Ser13=)	rs336283	0.73657
NM_001077653.2(TBX20):c.765C>A (p.Ile255=)	rs6950175	0.02695
NM_001077653.2(TBX20):c.1017A>C (p.Thr339=)	rs112054378	0.00547
NM_001077653.2(TBX20):c.501C>T (p.Ser167=)	rs75947625	0.00088

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