List of variants in gene TGFB3 reported as benign for long QT syndrome

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_003239.5(TGFB3):c.293C>T (p.Ser98Leu)	rs142047577	0.00092

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