List of variants reported as benign for Loeys-Dietz syndrome 4 by Illumina Laboratory Services, Illumina

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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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.*747A>C	rs991967	0.37303
NM_003238.6(TGFB2):c.*2431C>G	rs1046017	0.37219
NM_003238.6(TGFB2):c.*1310C>T	rs1418556	0.37003
NM_003238.6(TGFB2):c.*2839G>A	rs6704255	0.35183
NM_003238.6(TGFB2):c.*3196C>T	rs6683598	0.34937
NM_003238.6(TGFB2):c.*201A>T	rs900	0.32524
NM_003238.6(TGFB2):c.-714A>C	rs73110310	0.10708
NM_003238.6(TGFB2):c.*1624T>A	rs3737977	0.10338
NM_003238.6(TGFB2):c.-1302A>G	rs10482718	0.03064
NM_003238.6(TGFB2):c.*39G>A	rs11466412	0.02203
NM_003238.6(TGFB2):c.*1443T>A	rs60086269	0.01705
NM_003238.6(TGFB2):c.643+7A>C	rs7531245	0.01418
NM_003238.6(TGFB2):c.*1585C>G	rs17047863	0.00958
NM_003238.6(TGFB2):c.-1230G>A	rs11466363	0.00928
NM_003238.6(TGFB2):c.*969T>C	rs187495965	0.00490
NM_003238.6(TGFB2):c.*1684G>C	rs192396801	0.00452
NM_003238.6(TGFB2):c.272G>A (p.Arg91His)	rs10482721	0.00297
NM_003238.6(TGFB2):c.*2269T>C	rs193244018	0.00262
NM_003238.6(TGFB2):c.-746G>T	rs576053414	0.00259
NM_003238.6(TGFB2):c.*1315T>G	rs577782618	0.00214
NM_003238.6(TGFB2):c.*720T>C	rs544540486	0.00087
NM_003238.6(TGFB2):c.114G>A (p.Glu38=)	rs149215818	0.00087
NM_003238.6(TGFB2):c.*2950G>A	rs147957308	0.00071
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.*135G>A	rs61762489	0.00049
NM_003238.6(TGFB2):c.356C>T (p.Pro119Leu)	rs149533093	0.00047
NM_003238.6(TGFB2):c.*2108G>A	rs184256338	0.00018
NM_003238.6(TGFB2):c.*1389C>T	rs528922293	0.00004
NM_003238.6(TGFB2):c.37C>A (p.His13Asn)	rs763918203	0.00001
NM_003238.6(TGFB2):c.*1198A>G	rs556560548
NM_003238.6(TGFB2):c.*2008G>A	rs12408711

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