ClinVar Miner

List of variants in gene TGFB2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_003238.6(TGFB2):c.-1302A>G rs10482718 0.03064
NM_003238.6(TGFB2):c.346+198T>G rs1106569 0.03058
NM_003238.6(TGFB2):c.*39G>A rs11466412 0.02203
NM_003238.6(TGFB2):c.511-127C>A rs10482808 0.01735
NM_003238.6(TGFB2):c.754+58A>G rs10482811 0.01102
NM_003238.6(TGFB2):c.511-73G>C rs10482809 0.01100
NM_003238.6(TGFB2):c.-620G>A rs886045971 0.01029
NM_003238.6(TGFB2):c.-1230G>A rs11466363 0.00928
NM_003238.6(TGFB2):c.755-206C>A rs10482816 0.00919
NM_003238.6(TGFB2):c.-288A>T rs116531760 0.00572
NM_003238.6(TGFB2):c.346+16454G>A rs11466375 0.00455
NM_003238.6(TGFB2):c.823A>G (p.Ser275Gly) rs139825195 0.00062
NM_003238.6(TGFB2):c.356C>T (p.Pro119Leu) rs149533093 0.00047
NM_003238.6(TGFB2):c.588C>T (p.Gly196=) rs192335285 0.00038
NM_003238.6(TGFB2):c.747A>G (p.Arg249=) rs147960792 0.00032
NM_003238.6(TGFB2):c.648G>A (p.Arg216=) rs767503001 0.00012
NM_003238.6(TGFB2):c.297C>T (p.Tyr99=) rs760759052 0.00011
NM_003238.6(TGFB2):c.1140C>T (p.Cys380=) rs201129153 0.00006
NM_003238.6(TGFB2):c.644-4C>T rs11466408 0.00006
NM_003238.6(TGFB2):c.1008C>T (p.His336=) rs886038528 0.00005
NM_003238.6(TGFB2):c.-6T>A rs772514115 0.00004
NM_003238.6(TGFB2):c.555C>T (p.Ile185=) rs760740958 0.00004
NM_003238.6(TGFB2):c.603C>T (p.Phe201=) rs377264861 0.00004
NM_003238.6(TGFB2):c.-16T>C rs779785854 0.00003
NM_003238.6(TGFB2):c.798T>A (p.Thr266=) rs376354795 0.00002
NM_003238.6(TGFB2):c.*15T>C rs1057520937 0.00001
NM_003238.6(TGFB2):c.*9G>A rs1057521805 0.00001
NM_003238.6(TGFB2):c.501G>A (p.Glu167=) rs550789732 0.00001
NM_003238.6(TGFB2):c.942G>A (p.Gln314=) rs188801474 0.00001
NM_003238.6(TGFB2):c.-45dup rs200186989
NM_003238.6(TGFB2):c.-4A>C rs1571820524
NM_003238.6(TGFB2):c.1086+19T>C rs1553303372
NM_003238.6(TGFB2):c.1087-14C>T rs1341545472
NM_003238.6(TGFB2):c.346+8C>T rs1553292149
NM_003238.6(TGFB2):c.375C>G (p.Pro125=) rs1658868131
NM_003238.6(TGFB2):c.510+12TTG[11] rs10482769
NM_003238.6(TGFB2):c.510+53CT[10] rs142802402
NM_003238.6(TGFB2):c.511-10del rs376560786
NM_003238.6(TGFB2):c.644-18T>A rs1553302992
NM_003238.6(TGFB2):c.754+10dup rs1553303016
NM_003238.6(TGFB2):c.837A>G (p.Pro279=) rs1553303186
NM_003238.6(TGFB2):c.870A>G (p.Arg290=) rs1057521201
NM_003238.6(TGFB2):c.933-6del rs11285412

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