List of variants in gene TGFBR2 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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.106A>G (p.Met36Val)	rs17025864	0.00092
NM_003242.6(TGFBR2):c.4G>T (p.Gly2Cys)	rs565502802	0.00021
NM_003242.6(TGFBR2):c.567C>T (p.Tyr189=)	rs371221124	0.00005
NM_003242.6(TGFBR2):c.1015C>T (p.Arg339Trp)	rs761991787	0.00004
NM_003242.6(TGFBR2):c.81C>T (p.His27=)	rs1057520957	0.00003
NM_003242.6(TGFBR2):c.1185G>C (p.Leu395=)	rs193922663	0.00001
NM_003242.6(TGFBR2):c.1263T>G (p.Thr421=)	rs1397322686	0.00001
NM_003242.6(TGFBR2):c.215G>A (p.Ser72Asn)	rs764941621
NM_003242.6(TGFBR2):c.516C>T (p.Leu172=)	rs1301321642
NM_003242.6(TGFBR2):c.721C>T (p.Leu241=)	rs2125434109
NM_003242.6(TGFBR2):c.78G>A (p.Pro26=)	rs753781287

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