List of variants in gene TGFB2 reported as benign by GeneDx

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_003238.6(TGFB2):c.-784A>C	rs1557153	0.99928
NM_003238.6(TGFB2):c.-677T>C	rs112369231	0.39003
NM_003238.6(TGFB2):c.932+213A>G	rs6684205	0.37235
NM_003238.6(TGFB2):c.*201A>T	rs900	0.32524
NC_000001.11:g.218345173A>C	rs7550232	0.19737
NM_003238.6(TGFB2):c.932+247G>A	rs10482819	0.03234
NM_003238.6(TGFB2):c.754+333G>T	rs10482813	0.01918
NM_003238.6(TGFB2):c.1087-207G>A	rs10482838	0.01708
NM_003238.6(TGFB2):c.933-251C>A	rs10482821	0.01616
NM_003238.6(TGFB2):c.754+71T>C	rs10482812	0.01612
NM_003238.6(TGFB2):c.643+7A>C	rs7531245	0.01418
NM_003238.6(TGFB2):c.1239C>T (p.Cys413=)	rs141225367	0.00359
NM_003238.6(TGFB2):c.619G>C (p.Val207Leu)	rs10482810	0.00359
NM_003238.6(TGFB2):c.272G>A (p.Arg91His)	rs10482721	0.00297
NM_003238.6(TGFB2):c.114G>A (p.Glu38=)	rs149215818	0.00087
NM_003238.6(TGFB2):c.303G>A (p.Lys101=)	rs147052890	0.00072
NM_003238.6(TGFB2):c.-5A>T	rs200702935	0.00060
NM_003238.6(TGFB2):c.357G>A (p.Pro119=)	rs138514914	0.00054
NM_003238.6(TGFB2):c.347-14C>G	rs371982231	0.00014
NC_000001.11:g.218345083CTTC[1]	rs9331507
NM_003238.6(TGFB2):c.-113_-110dup	rs10482719
NM_003238.6(TGFB2):c.-45del	rs200186989
NM_003238.6(TGFB2):c.1087-276dup	rs10482837
NM_003238.6(TGFB2):c.510+12TTG[12]	rs10482769
NM_003238.6(TGFB2):c.510+12TTG[13]	rs10482769
NM_003238.6(TGFB2):c.510+12TTG[9]	rs10482769
NM_003238.6(TGFB2):c.933-6del	rs11285412

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