ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 144
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HGVS dbSNP
NC_000005.10:g.128538265G>T rs142885655
NM_001999.4(FBN2):c.-262C>T rs540026322
NM_001999.4(FBN2):c.1040G>A (p.Arg347His) rs112428886
NM_001999.4(FBN2):c.1053C>T (p.Thr351=) rs1554067080
NM_001999.4(FBN2):c.1079-10A>G rs766920012
NM_001999.4(FBN2):c.1231+37C>G rs28763953
NM_001999.4(FBN2):c.1232-252A>G rs76328881
NM_001999.4(FBN2):c.1232-6T>C rs1581260490
NM_001999.4(FBN2):c.1256A>G (p.Asp419Gly) rs140464202
NM_001999.4(FBN2):c.1260A>C (p.Gly420=) rs766241911
NM_001999.4(FBN2):c.1338C>G (p.Gly446=) rs1060504933
NM_001999.4(FBN2):c.1422C>T (p.Ala474=) rs764073494
NM_001999.4(FBN2):c.1431G>A (p.Gly477=) rs759633050
NM_001999.4(FBN2):c.1465+271A>G rs76462170
NM_001999.4(FBN2):c.1466-4G>A rs371636769
NM_001999.4(FBN2):c.147C>T (p.Ser49=) rs1194404343
NM_001999.4(FBN2):c.150T>C (p.Ala50=) rs543546489
NM_001999.4(FBN2):c.1716A>G (p.Ala572=) rs771782180
NM_001999.4(FBN2):c.1724-4C>A rs886432251
NM_001999.4(FBN2):c.1776G>A (p.Val592=) rs775492838
NM_001999.4(FBN2):c.1849+149A>G rs112258148
NM_001999.4(FBN2):c.1849+96G>A rs116773938
NM_001999.4(FBN2):c.2095+7_2095+20del rs1178750566
NM_001999.4(FBN2):c.2096-256G>A rs115515304
NM_001999.4(FBN2):c.2096-306A>C rs115985327
NM_001999.4(FBN2):c.209T>C (p.Val70Ala) rs144149249
NM_001999.4(FBN2):c.2199A>G (p.Pro733=)
NM_001999.4(FBN2):c.2214A>T (p.Gly738=) rs201548788
NM_001999.4(FBN2):c.2248+283A>G rs144388289
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.2340C>T (p.Ala780=) rs1060504935
NM_001999.4(FBN2):c.2427T>A (p.Ile809=) rs139686090
NM_001999.4(FBN2):c.2429-11G>A rs201849584
NM_001999.4(FBN2):c.2439A>G (p.Glu813=) rs1581241374
NM_001999.4(FBN2):c.2457G>A (p.Leu819=)
NM_001999.4(FBN2):c.2469C>T (p.Asn823=) rs770997817
NM_001999.4(FBN2):c.2487G>A (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.2634G>T (p.Ser878=) rs143905167
NM_001999.4(FBN2):c.2674+10A>G rs371734006
NM_001999.4(FBN2):c.2864-102T>C rs114090698
NM_001999.4(FBN2):c.2902A>G (p.Asn968Asp) rs774248421
NM_001999.4(FBN2):c.294C>T (p.Cys98=) rs765214316
NM_001999.4(FBN2):c.2989+14C>T rs775432537
NM_001999.4(FBN2):c.2990-7G>C rs1245936560
NM_001999.4(FBN2):c.3045C>G (p.Pro1015=) rs371640952
NM_001999.4(FBN2):c.3147G>A (p.Glu1049=) rs1356177204
NM_001999.4(FBN2):c.3217+13G>C rs572013507
NM_001999.4(FBN2):c.3222C>A (p.Ile1074=) rs1345516642
NM_001999.4(FBN2):c.3343+266G>A rs141806441
NM_001999.4(FBN2):c.337+185A>G rs76039082
NM_001999.4(FBN2):c.3393C>T (p.Cys1131=) rs760695805
NM_001999.4(FBN2):c.3420C>T (p.Cys1140=) rs756541654
NM_001999.4(FBN2):c.3432A>G (p.Glu1144=) rs757682009
NM_001999.4(FBN2):c.3598+40A>G rs182112935
NM_001999.4(FBN2):c.3693T>C (p.Tyr1231=) rs1561776923
NM_001999.4(FBN2):c.3724+57C>T rs75170825
NM_001999.4(FBN2):c.3973+96_3973+98del rs547745692
NM_001999.4(FBN2):c.4002T>C (p.Asn1334=) rs759408247
NM_001999.4(FBN2):c.4134C>T (p.Cys1378=) rs775405425
NM_001999.4(FBN2):c.4222+10C>A rs376700480
NM_001999.4(FBN2):c.42G>T (p.Leu14=) rs376407285
NM_001999.4(FBN2):c.4345+324T>C rs116561386
NM_001999.4(FBN2):c.4515A>G (p.Thr1505=) rs751938197
NM_001999.4(FBN2):c.4590T>C (p.Cys1530=) rs1581212624
NM_001999.4(FBN2):c.4677A>G (p.Pro1559=) rs1581212135
NM_001999.4(FBN2):c.4680C>T (p.Pro1560=) rs377502943
NM_001999.4(FBN2):c.4773G>A (p.Leu1591=) rs753387547
NM_001999.4(FBN2):c.4779C>T (p.Cys1593=) rs780191346
NM_001999.4(FBN2):c.4879+7A>G rs555328744
NM_001999.4(FBN2):c.4880-12A>G rs376111927
NM_001999.4(FBN2):c.4902C>T (p.Pro1634=) rs201071253
NM_001999.4(FBN2):c.4914C>T (p.Gly1638=) rs1482008222
NM_001999.4(FBN2):c.4983C>T (p.Cys1661=) rs143907156
NM_001999.4(FBN2):c.5004C>T (p.Asn1668=) rs140012679
NM_001999.4(FBN2):c.5031C>T (p.Cys1677=) rs147452231
NM_001999.4(FBN2):c.5075-7A>C rs946913190
NM_001999.4(FBN2):c.5118G>A (p.Gly1706=) rs1284156837
NM_001999.4(FBN2):c.5295A>C (p.Thr1765=) rs941916367
NM_001999.4(FBN2):c.5307C>A (p.Gly1769=) rs755781072
NM_001999.4(FBN2):c.533-4G>T rs372596001
NM_001999.4(FBN2):c.533-92A>G rs112355068
NM_001999.4(FBN2):c.5353+10C>A rs113589974
NM_001999.4(FBN2):c.5637C>T (p.Ala1879=) rs367620361
NM_001999.4(FBN2):c.5682T>C (p.Asn1894=) rs991908659
NM_001999.4(FBN2):c.5703C>T (p.Asn1901=) rs746592808
NM_001999.4(FBN2):c.5731C>T (p.Leu1911=) rs768733086
NM_001999.4(FBN2):c.573C>T (p.Ile191=) rs370698125
NM_001999.4(FBN2):c.5917+201T>A rs26023
NM_001999.4(FBN2):c.6291T>G (p.Phe2097Leu) rs898218975
NM_001999.4(FBN2):c.6293-8T>A rs375682913
NM_001999.4(FBN2):c.6411G>A (p.Gly2137=) rs552637321
NM_001999.4(FBN2):c.6445+11T>C rs766726816
NM_001999.4(FBN2):c.6446T>C (p.Val2149Ala) rs191065419
NM_001999.4(FBN2):c.6637+39A>G rs17608435
NM_001999.4(FBN2):c.6637+8T>C rs780697390
NM_001999.4(FBN2):c.6765C>T (p.Asn2255=) rs140044610
NM_001999.4(FBN2):c.6833C>T (p.Thr2278Met) rs2307109
NM_001999.4(FBN2):c.685C>T (p.Leu229=) rs200698449
NM_001999.4(FBN2):c.6948C>T (p.Ile2316=) rs17608368
NM_001999.4(FBN2):c.6972T>C (p.Pro2324=) rs1581188714
NM_001999.4(FBN2):c.6982G>T (p.Ala2328Ser) rs199910288
NM_001999.4(FBN2):c.6984C>T (p.Ala2328=) rs942158485
NM_001999.4(FBN2):c.7012+8G>A rs1422660066
NM_001999.4(FBN2):c.7137T>G (p.Leu2379=) rs765676702
NM_001999.4(FBN2):c.7139-33G>A rs199889927
NM_001999.4(FBN2):c.7181T>C (p.Ile2394Thr) rs28763926
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.7345+9T>C rs1212635601
NM_001999.4(FBN2):c.7346-196C>T rs140756341
NM_001999.4(FBN2):c.7374C>T (p.Asn2458=) rs1383809012
NM_001999.4(FBN2):c.7471+21A>G rs28763924
NM_001999.4(FBN2):c.7539T>C (p.Tyr2513=) rs1581181343
NM_001999.4(FBN2):c.7595-139A>G rs73341402
NM_001999.4(FBN2):c.7655G>A (p.Gly2552Glu) rs1473525001
NM_001999.4(FBN2):c.7719C>T (p.Asn2573=) rs746265117
NM_001999.4(FBN2):c.7740G>A (p.Ser2580=) rs942206547
NM_001999.4(FBN2):c.7767A>G (p.Gln2589=)
NM_001999.4(FBN2):c.778C>G (p.Pro260Ala) rs774323549
NM_001999.4(FBN2):c.7960+208C>T rs73341388
NM_001999.4(FBN2):c.8112C>T (p.Asn2704=) rs370851605
NM_001999.4(FBN2):c.8192+244C>T rs41298328
NM_001999.4(FBN2):c.8192+8G>A rs184132548
NM_001999.4(FBN2):c.8253C>T (p.Val2751=) rs140631421
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.8322C>T (p.Asp2774=) rs1554115402
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.8490C>T (p.Asn2830=) rs1581170322
NM_001999.4(FBN2):c.8520C>T (p.Asn2840=) rs139098335
NM_001999.4(FBN2):c.8559C>T (p.Leu2853=) rs778576181
NM_001999.4(FBN2):c.885A>G (p.Thr295=) rs989219711
NM_001999.4(FBN2):c.891C>A (p.Gly297=) rs539258943
NM_001999.4(FBN2):c.960T>C (p.Asp320=) rs1581270421

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