List of variants in gene TGFB3 reported as benign

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_003239.5(TGFB3):c.926+290G>T	rs2359994	0.84966
NM_003239.5(TGFB3):c.754+257A>G	rs3917192	0.82708
NM_003239.5(TGFB3):c.926+104G>A	rs3917201	0.70713
NM_003239.5(TGFB3):c.647-98A>G	rs3917187	0.64994
NM_003239.5(TGFB3):c.755-38T>C	rs3917200	0.14180
NM_003239.5(TGFB3):c.352+236T>C	rs3917147	0.11929
NM_003239.5(TGFB3):c.754+139A>G	rs3917190	0.04365
NM_003239.5(TGFB3):c.*666A>G	rs4252348	0.02476
NM_003239.5(TGFB3):c.*696T>C	rs10129478	0.01788
NM_003239.5(TGFB3):c.516+135T>C	rs3917175	0.01560
NM_003239.5(TGFB3):c.1122C>G (p.Ala374=)	rs4252345	0.01156
NM_003239.5(TGFB3):c.*9G>A	rs4252346	0.00679
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.164G>A (p.Ser55Asn)	rs143229915	0.00100
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.504C>T (p.Ile168=)	rs148029842	0.00006
NM_003239.5(TGFB3):c.96C>T (p.Phe32=)	rs748977151	0.00006
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.*482del	rs199646113
NM_003239.5(TGFB3):c.647-80del	rs3917188
NM_003239.5(TGFB3):c.921C>T (p.Cys307=)	rs575379914
NM_003239.5(TGFB3):c.927-13dup	rs1303198865

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