List of variants in gene TGFBR2 reported as benign by Invitae

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: 26

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HGVS	dbSNP	gnomAD frequency
NC_000003.12:g.30605668A>G	rs3087465	0.64037
NM_003242.6(TGFBR2):c.263+7A>G	rs1155705	0.34308
NM_003242.6(TGFBR2):c.95-1332C>T	rs17838698	0.30717
NM_003242.6(TGFBR2):c.455-4T>A	rs11466512	0.25954
NC_000003.12:g.30694445G>A	rs744751	0.22965
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.1602G>A (p.Val534=)	rs140818646	0.00166
NM_003242.6(TGFBR2):c.1657T>A (p.Ser553Thr)	rs112215250	0.00115
NM_003242.6(TGFBR2):c.1458C>T (p.Ser486=)	rs139881155	0.00075
NM_003242.6(TGFBR2):c.571G>A (p.Val191Ile)	rs56105708	0.00039
NM_003242.6(TGFBR2):c.944C>T (p.Thr315Met)	rs34833812	0.00034
NM_003242.6(TGFBR2):c.915C>T (p.Leu305=)	rs146030104	0.00026
NM_003242.6(TGFBR2):c.1254+16T>C	rs45515293	0.00014
NM_003242.6(TGFBR2):c.95-7T>C	rs764533083	0.00005
NM_003242.6(TGFBR2):c.690G>A (p.Thr230=)	rs201560560	0.00003
NM_003242.6(TGFBR2):c.927G>A (p.Thr309=)	rs756625146	0.00002
NM_003242.6(TGFBR2):c.115A>T (p.Thr39Ser)	rs780280433	0.00001
NM_003242.6(TGFBR2):c.1159G>T (p.Val387Leu)	rs35766612
NM_003242.6(TGFBR2):c.263+17del	rs754721647
NM_003242.6(TGFBR2):c.455-14del	rs2125433170
NM_003242.6(TGFBR2):c.94+16299A>C	rs184395862
NM_003242.6(TGFBR2):c.95-3300G>C	rs12493607

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