List of variants in gene TGFBR1 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004612.4(TGFBR1):c.528G>A (p.Thr176=)	rs190878719	0.00026
NM_004612.4(TGFBR1):c.1032T>C (p.Asn344=)	rs192662552	0.00022
NM_004612.4(TGFBR1):c.1216T>C (p.Leu406=)	rs200062984	0.00016
NM_004612.4(TGFBR1):c.120C>T (p.Leu40=)	rs201267786	0.00011
NM_004612.4(TGFBR1):c.1387-4G>A	rs397517031

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