List of variants in gene TGFB2 reported as likely benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_003238.6(TGFB2):c.*1128G>A	rs56271792	0.01172
NM_003238.6(TGFB2):c.-1016C>T	rs11466365	0.01071
NM_003238.6(TGFB2):c.-288A>T	rs116531760	0.00572
NM_003238.6(TGFB2):c.619G>C (p.Val207Leu)	rs10482810	0.00359
NM_003238.6(TGFB2):c.*1233T>A	rs555872587	0.00091
NM_003238.6(TGFB2):c.798T>A (p.Thr266=)	rs376354795	0.00002
NM_003238.6(TGFB2):c.*1233del	rs532376886
NM_003238.6(TGFB2):c.*21G>T	rs778452299
NM_003238.6(TGFB2):c.-45del	rs200186989
NM_003238.6(TGFB2):c.-644AC[11]	rs151329324

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