List of variants in gene TGFBR2 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 11

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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.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.1525-8C>T	rs11466530	0.00230
NM_003242.6(TGFBR2):c.1062C>T (p.Leu354=)	rs113194608	0.00194
NM_003242.6(TGFBR2):c.1119G>A (p.Met373Ile)	rs35719192	0.00130
NM_003242.6(TGFBR2):c.94+16202A>G	rs375610471	0.00039
NM_003242.6(TGFBR2):c.1254+16T>C	rs45515293	0.00014
NM_003242.6(TGFBR2):c.383del (p.Lys128fs)	rs79375991

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