List of variants in gene TGFBR2 reported as likely pathogenic 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003242.6(TGFBR2):c.1063G>C (p.Ala355Pro)	rs104893813
NM_003242.6(TGFBR2):c.1151A>G (p.Asn384Ser)	rs193922660
NM_003242.6(TGFBR2):c.1540T>C (p.Cys514Arg)	rs193922664
NM_003242.6(TGFBR2):c.1580C>T (p.Ala527Val)	rs727503476
NM_003242.6(TGFBR2):c.310C>T (p.Pro104Ser)	rs193922665
NM_003242.6(TGFBR2):c.902A>G (p.His301Arg)	rs863223857

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