ClinVar Miner

List of variants in gene FBN2 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP
NC_000005.10:g.128538274A>G rs138741640
NC_000005.10:g.128538300G>C rs141359565
NM_001999.4(FBN2):c.-435C>T rs78230270
NM_001999.4(FBN2):c.-511G>A rs7712942
NM_001999.4(FBN2):c.-625G>C rs147684576
NM_001999.4(FBN2):c.1040G>A (p.Arg347His) rs112428886
NM_001999.4(FBN2):c.1465+54A>G rs73345284
NM_001999.4(FBN2):c.1749G>A (p.Gly583=) rs75940000
NM_001999.4(FBN2):c.2096-224A>G rs331098
NM_001999.4(FBN2):c.2302+260T>G rs1428632
NM_001999.4(FBN2):c.2303-276G>T rs552850
NM_001999.4(FBN2):c.254+274T>C rs73348280
NM_001999.4(FBN2):c.254+303C>G rs73348278
NM_001999.4(FBN2):c.2555-287A>T rs3816905
NM_001999.4(FBN2):c.2674+147A>G rs27457
NM_001999.4(FBN2):c.2812+182A>G rs151987
NM_001999.4(FBN2):c.2856G>T (p.Thr952=) rs556038110
NM_001999.4(FBN2):c.2863+23G>T rs255690
NM_001999.4(FBN2):c.2893G>A (p.Val965Ile) rs154001
NM_001999.4(FBN2):c.2990-298C>T rs468182
NM_001999.4(FBN2):c.3015G>A (p.Leu1005=) rs28763946
NM_001999.4(FBN2):c.3217+231G>A rs468026
NM_001999.4(FBN2):c.3344-264G>A rs115736330
NM_001999.4(FBN2):c.338-89C>A rs58297481
NM_001999.4(FBN2):c.3473-318C>T rs27859
NM_001999.4(FBN2):c.3599-119T>C rs32221
NM_001999.4(FBN2):c.3974-67G>A rs28763944
NM_001999.4(FBN2):c.4100-216C>A rs458882
NM_001999.4(FBN2):c.4100-265G>A rs32235
NM_001999.4(FBN2):c.4100-9G>T rs377002313
NM_001999.4(FBN2):c.4223-178A>G rs469722
NM_001999.4(FBN2):c.4312G>A (p.Glu1438Lys) rs56168072
NM_001999.4(FBN2):c.4345+183A>G rs469913
NM_001999.4(FBN2):c.4345+329C>T rs467928
NM_001999.4(FBN2):c.437-162A>G rs114070767
NM_001999.4(FBN2):c.4717+285T>C rs414540
NM_001999.4(FBN2):c.4879+138C>T rs461146
NM_001999.4(FBN2):c.4879+269T>C rs10076728
NM_001999.4(FBN2):c.5074+298A>T rs612993
NM_001999.4(FBN2):c.5200+148A>G rs76244360
NM_001999.4(FBN2):c.5200+286A>G rs10040006
NM_001999.4(FBN2):c.5201-196A>T rs469294
NM_001999.4(FBN2):c.533-96_533-92del rs3059402
NM_001999.4(FBN2):c.5422+154G>A rs17839648
NM_001999.4(FBN2):c.5423-276G>T rs32220
NM_001999.4(FBN2):c.5675-87T>C rs27855
NM_001999.4(FBN2):c.5823T>C (p.His1941=) rs11955288
NM_001999.4(FBN2):c.5917+112A>G rs28763937
NM_001999.4(FBN2):c.5917+201T>G rs26023
NM_001999.4(FBN2):c.5918-327C>T rs12523609
NM_001999.4(FBN2):c.6138G>T (p.Gly2046=) rs150627604
NM_001999.4(FBN2):c.628+118A>T rs6886186
NM_001999.4(FBN2):c.628+208G>A rs6864831
NM_001999.4(FBN2):c.6292+12C>A rs10042349
NM_001999.4(FBN2):c.6292+303A>T rs6871353
NM_001999.4(FBN2):c.6293-308C>T rs11241955
NM_001999.4(FBN2):c.6511+15A>G rs56131649
NM_001999.4(FBN2):c.6511+5G>A rs200608284
NM_001999.4(FBN2):c.6757+309A>T rs6884264
NM_001999.4(FBN2):c.6758-308A>G rs42280
NM_001999.4(FBN2):c.6880+17G>A rs2042327
NM_001999.4(FBN2):c.6881-107C>T rs10070948
NM_001999.4(FBN2):c.6881-206G>T rs11746935
NM_001999.4(FBN2):c.6931A>G (p.Met2311Val) rs32209
NM_001999.4(FBN2):c.6948C>A (p.Ile2316=) rs17608368
NM_001999.4(FBN2):c.7013-5T>C rs28763927
NM_001999.4(FBN2):c.7263G>A (p.Gln2421=) rs114376818
NM_001999.4(FBN2):c.728T>C (p.Ile243Thr) rs117524265
NM_001999.4(FBN2):c.7346-94G>C rs426987
NM_001999.4(FBN2):c.7471+273C>A rs255695
NM_001999.4(FBN2):c.7594+231T>A rs1428633
NM_001999.4(FBN2):c.7711+257G>A rs2307108
NM_001999.4(FBN2):c.7739C>T (p.Ser2580Leu) rs2291628
NM_001999.4(FBN2):c.7840+288A>G rs72785104
NM_001999.4(FBN2):c.7841-322T>C rs75856965
NM_001999.4(FBN2):c.8154C>T (p.Leu2718=) rs34119447
NM_001999.4(FBN2):c.8274C>T (p.Ser2758=) rs10070365
NM_001999.4(FBN2):c.8351C>T (p.Pro2784Leu) rs144574441
NM_001999.4(FBN2):c.8733C>G (p.Leu2911=) rs34383505
NM_001999.4(FBN2):c.953-333G>A rs3805648
NM_001999.4(FBN2):c.976C>T (p.Pro326Ser) rs28763954

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