List of variants in gene TGFB3 reported as benign for cardiovascular disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_003239.5(TGFB3):c.1122C>G (p.Ala374=)	rs4252345	0.01156
NM_003239.5(TGFB3):c.39C>T (p.Ala13=)	rs11466415	0.00461
NM_003239.5(TGFB3):c.744C>A (p.Ile248=)	rs45477900	0.00123
NM_003239.5(TGFB3):c.34C>T (p.Leu12=)	rs143612445	0.00096
NM_003239.5(TGFB3):c.293C>T (p.Ser98Leu)	rs142047577	0.00092
NM_003239.5(TGFB3):c.517-16T>C	rs3917176	0.00050
NM_003239.5(TGFB3):c.647-12C>G	rs61762490	0.00023
NM_003239.5(TGFB3):c.88T>C (p.Leu30=)	rs3917145	0.00013
NM_003239.5(TGFB3):c.1081-14A>G	rs201379167	0.00005
NM_003239.5(TGFB3):c.288C>T (p.Thr96=)	rs201047560	0.00004
NM_003239.5(TGFB3):c.387C>T (p.Ser129=)	rs749768136	0.00004
NM_003239.5(TGFB3):c.927-20A>G	rs574227787	0.00002
NM_003239.5(TGFB3):c.798C>T (p.Arg266=)	rs772654040	0.00001
NM_003239.5(TGFB3):c.921C>T (p.Cys307=)	rs575379914
NM_003239.5(TGFB3):c.927-13dup	rs1303198865

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