List of variants in gene TGFBR2 reported as benign for Loeys-Dietz syndrome 2

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003242.6(TGFBR2):c.263+7A>G	rs1155705	0.34308
NM_003242.6(TGFBR2):c.455-4T>A	rs11466512	0.25954
NM_003242.6(TGFBR2):c.*747C>G	rs11466531	0.10463
NM_003242.6(TGFBR2):c.*1809A>G	rs6550008	0.07275
NM_003242.6(TGFBR2):c.*1521G>A	rs11466533	0.04903
NM_003242.6(TGFBR2):c.*2085T>A	rs11466537	0.04867
NM_003242.6(TGFBR2):c.1167C>T (p.Asn389=)	rs2228048	0.03013
NM_003242.6(TGFBR2):c.1266A>G (p.Ala422=)	rs2228047	0.02974
NM_003242.6(TGFBR2):c.999A>G (p.Leu333=)	rs2229102	0.02537
NM_003242.6(TGFBR2):c.1062C>T (p.Leu354=)	rs113194608	0.00194
NM_003242.6(TGFBR2):c.1602G>A (p.Val534=)	rs140818646	0.00166
NM_003242.6(TGFBR2):c.*2065C>T	rs11466536
NM_003242.6(TGFBR2):c.454+11T>C

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