ClinVar Miner

List of variants in gene FBN2 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 189
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HGVS dbSNP
NC_000005.10:g.128538265G>T rs142885655
NM_001999.4(FBN2):c.-17C>G rs372089451
NM_001999.4(FBN2):c.-262C>T rs540026322
NM_001999.4(FBN2):c.-33C>A rs1057521647
NM_001999.4(FBN2):c.1053C>T (p.Thr351=) rs1554067080
NM_001999.4(FBN2):c.1078+12A>C rs769211487
NM_001999.4(FBN2):c.1078+20G>A rs1057524321
NM_001999.4(FBN2):c.1079-14T>G rs754310681
NM_001999.4(FBN2):c.110C>A (p.Pro37Gln) rs201255083
NM_001999.4(FBN2):c.1167C>T (p.Cys389=) rs757599652
NM_001999.4(FBN2):c.1231+37C>G rs28763953
NM_001999.4(FBN2):c.1232-252A>G rs76328881
NM_001999.4(FBN2):c.132G>C (p.Pro44=) rs199702573
NM_001999.4(FBN2):c.1338C>G (p.Gly446=) rs1060504933
NM_001999.4(FBN2):c.1398C>T (p.Gly466=) rs1554066010
NM_001999.4(FBN2):c.1410C>T (p.Gly470=) rs750103822
NM_001999.4(FBN2):c.142C>A (p.Arg48=) rs1409799200
NM_001999.4(FBN2):c.1465+271A>G rs76462170
NM_001999.4(FBN2):c.1466-4G>A rs371636769
NM_001999.4(FBN2):c.1592G>C (p.Gly531Ala) rs34450503
NM_001999.4(FBN2):c.1724-4C>A rs886432251
NM_001999.4(FBN2):c.1849+12G>A rs777910433
NM_001999.4(FBN2):c.1849+149A>G rs112258148
NM_001999.4(FBN2):c.1849+96G>A rs116773938
NM_001999.4(FBN2):c.1973-20T>C rs774598343
NM_001999.4(FBN2):c.2013G>A (p.Gly671=) rs778762668
NM_001999.4(FBN2):c.2095+7_2095+22delinsT rs1064794511
NM_001999.4(FBN2):c.2096-13del rs746826953
NM_001999.4(FBN2):c.2096-256G>A rs115515304
NM_001999.4(FBN2):c.2096-306A>C rs115985327
NM_001999.4(FBN2):c.2160C>T (p.Pro720=) rs889188442
NM_001999.4(FBN2):c.2248+283A>G rs144388289
NM_001999.4(FBN2):c.2249-15C>A rs759195113
NM_001999.4(FBN2):c.2249-195T>C rs140295103
NM_001999.4(FBN2):c.2249-19A>G rs193091226
NM_001999.4(FBN2):c.2260G>A (p.Gly754Ser) rs145259927
NM_001999.4(FBN2):c.2303-284T>C rs114102715
NM_001999.4(FBN2):c.2358C>T (p.Asn786=) rs371981691
NM_001999.4(FBN2):c.2429-11G>A rs201849584
NM_001999.4(FBN2):c.2469C>T (p.Asn823=) rs770997817
NM_001999.4(FBN2):c.2487G>T (p.Thr829=) rs779455710
NM_001999.4(FBN2):c.254+322G>A rs567063128
NM_001999.4(FBN2):c.2555-184T>G rs62375019
NM_001999.4(FBN2):c.2634G>A (p.Ser878=) rs143905167
NM_001999.4(FBN2):c.2674+10A>G rs371734006
NM_001999.4(FBN2):c.2772C>T (p.Leu924=) rs773453872
NM_001999.4(FBN2):c.2802G>A (p.Arg934=) rs140500093
NM_001999.4(FBN2):c.2856G>T (p.Thr952=) rs556038110
NM_001999.4(FBN2):c.2864-102T>C rs114090698
NM_001999.4(FBN2):c.2864-12A>G rs1234935460
NM_001999.4(FBN2):c.2989+14C>T rs775432537
NM_001999.4(FBN2):c.2989+20G>A rs374450061
NM_001999.4(FBN2):c.2990-7G>C rs1245936560
NM_001999.4(FBN2):c.2990-8C>T rs370825177
NM_001999.4(FBN2):c.3217+12C>A rs375688726
NM_001999.4(FBN2):c.3217+13G>C rs572013507
NM_001999.4(FBN2):c.3217+18G>A rs1554123696
NM_001999.4(FBN2):c.3222C>A (p.Ile1074=) rs1345516642
NM_001999.4(FBN2):c.3235G>T (p.Ala1079Ser) rs774996980
NM_001999.4(FBN2):c.3343+266G>A rs141806441
NM_001999.4(FBN2):c.337+185A>G rs76039082
NM_001999.4(FBN2):c.339G>A (p.Pro113=) rs144540627
NM_001999.4(FBN2):c.3414T>C (p.Phe1138=) rs769005512
NM_001999.4(FBN2):c.3472+17C>A rs747730357
NM_001999.4(FBN2):c.3518C>G (p.Thr1173Ser) rs199678757
NM_001999.4(FBN2):c.3598+40A>G rs182112935
NM_001999.4(FBN2):c.3655A>G (p.Met1219Val) rs201288931
NM_001999.4(FBN2):c.3690A>G (p.Gly1230=) rs774807410
NM_001999.4(FBN2):c.3724+57C>T rs75170825
NM_001999.4(FBN2):c.3740T>C (p.Met1247Thr) rs149054177
NM_001999.4(FBN2):c.3750C>T (p.Asn1250=) rs750559514
NM_001999.4(FBN2):c.3767A>G (p.Gln1256Arg) rs139052603
NM_001999.4(FBN2):c.3847+5A>G rs1444917250
NM_001999.4(FBN2):c.3973+96_3973+98del rs547745692
NM_001999.4(FBN2):c.4100-9G>T rs377002313
NM_001999.4(FBN2):c.4222+10C>A rs376700480
NM_001999.4(FBN2):c.4223-14G>T rs370506719
NM_001999.4(FBN2):c.4230C>T (p.Asp1410=) rs138289440
NM_001999.4(FBN2):c.4296C>T (p.Tyr1432=) rs147046215
NM_001999.4(FBN2):c.42G>T (p.Leu14=) rs376407285
NM_001999.4(FBN2):c.4311C>T (p.Ser1437=) rs138665246
NM_001999.4(FBN2):c.4345+324T>C rs116561386
NM_001999.4(FBN2):c.436+20C>T rs1168120609
NM_001999.4(FBN2):c.4454A>G (p.Asp1485Gly) rs199665922
NM_001999.4(FBN2):c.4690T>C (p.Leu1564=) rs886038504
NM_001999.4(FBN2):c.4717+25_4717+28del rs1064795498
NM_001999.4(FBN2):c.4773G>T (p.Leu1591=) rs753387547
NM_001999.4(FBN2):c.477T>C (p.Cys159=) rs138601900
NM_001999.4(FBN2):c.4879+7A>G rs555328744
NM_001999.4(FBN2):c.4880-12A>G rs376111927
NM_001999.4(FBN2):c.4949-18C>G rs372234336
NM_001999.4(FBN2):c.4962C>T (p.Cys1654=) rs753935960
NM_001999.4(FBN2):c.5031C>T (p.Cys1677=) rs147452231
NM_001999.4(FBN2):c.5075-7A>C rs946913190
NM_001999.4(FBN2):c.518C>T (p.Thr173Ile) rs147157552
NM_001999.4(FBN2):c.5196C>T (p.Cys1732=) rs1554120180
NM_001999.4(FBN2):c.5201-3T>C rs1057521162
NM_001999.4(FBN2):c.5201-6A>G rs879942478
NM_001999.4(FBN2):c.533-4G>T rs372596001
NM_001999.4(FBN2):c.533-6A>G rs56400997
NM_001999.4(FBN2):c.533-92A>G rs112355068
NM_001999.4(FBN2):c.5353+20A>G rs759401474
NM_001999.4(FBN2):c.5424C>T (p.Asp1808=) rs774758393
NM_001999.4(FBN2):c.5487C>T (p.Gly1829=) rs375136629
NM_001999.4(FBN2):c.5548+20T>C rs372334617
NM_001999.4(FBN2):c.5548+9A>C rs1057522115
NM_001999.4(FBN2):c.5674+18T>G rs199749609
NM_001999.4(FBN2):c.5675-12_5675-11insG rs150372632
NM_001999.4(FBN2):c.5703C>T (p.Asn1901=) rs746592808
NM_001999.4(FBN2):c.5800+20C>T rs1554119695
NM_001999.4(FBN2):c.5814C>T (p.Cys1938=) rs753556200
NM_001999.4(FBN2):c.5914C>T (p.Leu1972=) rs1554119518
NM_001999.4(FBN2):c.5917+201T>A rs26023
NM_001999.4(FBN2):c.5918-10T>C rs547697385
NM_001999.4(FBN2):c.5918-5T>A rs1057524021
NM_001999.4(FBN2):c.6138G>T (p.Gly2046=) rs150627604
NM_001999.4(FBN2):c.6167-4G>A rs370981323
NM_001999.4(FBN2):c.6252C>T (p.Pro2084=) rs1057524589
NM_001999.4(FBN2):c.629-19T>C rs374428361
NM_001999.4(FBN2):c.6297T>C (p.Thr2099=) rs770778839
NM_001999.4(FBN2):c.6411G>A (p.Gly2137=) rs552637321
NM_001999.4(FBN2):c.6445+11T>C rs766726816
NM_001999.4(FBN2):c.6450A>T (p.Ala2150=) rs1199375914
NM_001999.4(FBN2):c.6477T>C (p.His2159=) rs768972914
NM_001999.4(FBN2):c.6511+4C>T rs368610241
NM_001999.4(FBN2):c.6512-7A>G rs201462445
NM_001999.4(FBN2):c.6534C>T (p.Ser2178=) rs1057524084
NM_001999.4(FBN2):c.6573C>T (p.Asp2191=) rs374456115
NM_001999.4(FBN2):c.6637+39A>G rs17608435
NM_001999.4(FBN2):c.6655A>G (p.Ile2219Val) rs140821039
NM_001999.4(FBN2):c.6669T>C (p.Cys2223=) rs754724355
NM_001999.4(FBN2):c.6765C>T (p.Asn2255=) rs140044610
NM_001999.4(FBN2):c.6840G>A (p.Pro2280=) rs377742525
NM_001999.4(FBN2):c.6841A>T (p.Ile2281Phe) rs115223340
NM_001999.4(FBN2):c.6903G>T (p.Gly2301=) rs886039130
NM_001999.4(FBN2):c.6948C>T (p.Ile2316=) rs17608368
NM_001999.4(FBN2):c.6990G>A (p.Arg2330=) rs28763928
NM_001999.4(FBN2):c.69G>T (p.Ala23=) rs774856011
NM_001999.4(FBN2):c.6G>C (p.Gly2=) rs746567292
NM_001999.4(FBN2):c.7012+6C>T rs749376421
NM_001999.4(FBN2):c.7013-18T>C rs375140877
NM_001999.4(FBN2):c.7013-7del rs1554117268
NM_001999.4(FBN2):c.7137T>G (p.Leu2379=) rs765676702
NM_001999.4(FBN2):c.7139-33G>A rs199889927
NM_001999.4(FBN2):c.7167G>A (p.Glu2389=) rs761050040
NM_001999.4(FBN2):c.7205G>A (p.Arg2402His) rs148014419
NM_001999.4(FBN2):c.7263G>A (p.Gln2421=) rs114376818
NM_001999.4(FBN2):c.7293C>T (p.Ala2431=) rs1057521075
NM_001999.4(FBN2):c.7346-196C>T rs140756341
NM_001999.4(FBN2):c.7471+21A>G rs28763924
NM_001999.4(FBN2):c.7472-17A>G rs773888786
NM_001999.4(FBN2):c.7587A>G (p.Thr2529=) rs145809024
NM_001999.4(FBN2):c.7594+12G>A rs184678810
NM_001999.4(FBN2):c.7595-139A>G rs73341402
NM_001999.4(FBN2):c.7595-18G>C rs1554116721
NM_001999.4(FBN2):c.7595-8A>G rs878854479
NM_001999.4(FBN2):c.7712-5G>A rs766722063
NM_001999.4(FBN2):c.7719C>T (p.Asn2573=) rs746265117
NM_001999.4(FBN2):c.7960+13T>G rs1023942727
NM_001999.4(FBN2):c.7960+208C>T rs73341388
NM_001999.4(FBN2):c.7961-19T>A rs1057524211
NM_001999.4(FBN2):c.7977C>G (p.Ser2659=) rs1057524372
NM_001999.4(FBN2):c.7A>C (p.Arg3=) rs1466844222
NM_001999.4(FBN2):c.8082C>T (p.His2694=) rs142755118
NM_001999.4(FBN2):c.8124C>T (p.Tyr2708=) rs201634501
NM_001999.4(FBN2):c.8139G>A (p.Thr2713=) rs1057523293
NM_001999.4(FBN2):c.8192+244C>T rs41298328
NM_001999.4(FBN2):c.8192+6G>A rs752575354
NM_001999.4(FBN2):c.8192+8G>A rs184132548
NM_001999.4(FBN2):c.8193-18T>A rs1057521159
NM_001999.4(FBN2):c.8193-6A>G rs371741283
NM_001999.4(FBN2):c.8196C>T (p.His2732=) rs780426123
NM_001999.4(FBN2):c.8253C>T (p.Val2751=) rs140631421
NM_001999.4(FBN2):c.8257G>A (p.Glu2753Lys) rs146781484
NM_001999.4(FBN2):c.827-263G>T rs141194324
NM_001999.4(FBN2):c.827-279G>A rs150728994
NM_001999.4(FBN2):c.8289C>T (p.Tyr2763=) rs190292877
NM_001999.4(FBN2):c.829G>A (p.Val277Ile) rs146849637
NM_001999.4(FBN2):c.8344C>T (p.His2782Tyr) rs745600341
NM_001999.4(FBN2):c.8364+18dup rs752497923
NM_001999.4(FBN2):c.8364+43A>G rs28763919
NM_001999.4(FBN2):c.8428T>A (p.Ser2810Thr) rs186577030
NM_001999.4(FBN2):c.8520C>T (p.Asn2840=) rs139098335
NM_001999.4(FBN2):c.8530G>A (p.Val2844Ile) rs147134796
NM_001999.4(FBN2):c.8559C>T (p.Leu2853=) rs778576181
NM_001999.4(FBN2):c.8595C>T (p.Pro2865=) rs137914321
NM_001999.4(FBN2):c.93G>T (p.Gln31His) rs371491169
NM_001999.4(FBN2):c.952+11C>T rs1157854895
NM_001999.4(FBN2):c.973A>G (p.Ile325Val) rs748879016

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