List of variants in gene TGFB3 reported as uncertain significance for Arrhythmogenic right ventricular dysplasia 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_003239.5(TGFB3):c.1169A>T (p.Tyr390Phe)	rs996297395	0.00013
NM_003239.5(TGFB3):c.559G>A (p.Gly187Ser)	rs201063101	0.00005
NM_003239.5(TGFB3):c.872C>T (p.Pro291Leu)	rs145121701	0.00004
NM_003239.5(TGFB3):c.488G>A (p.Arg163Gln)	rs920721092	0.00002
NM_003239.5(TGFB3):c.325G>A (p.Asp109Asn)	rs986180095
NM_003239.5(TGFB3):c.785G>T (p.Gly262Val)	rs1595339233
NM_003239.5(TGFB3):c.997G>A (p.Val333Ile)

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