ClinVar Miner

List of variants in gene FBN2 reported as uncertain significance for Cardiovascular phenotype

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 108
Download table as spreadsheet
HGVS dbSNP
NM_001999.4(FBN2):c.-2C>A rs776371080
NM_001999.4(FBN2):c.1126G>T (p.Ala376Ser) rs746951402
NM_001999.4(FBN2):c.1180C>T (p.Arg394Cys) rs563228953
NM_001999.4(FBN2):c.1234G>A (p.Glu412Lys) rs962522833
NM_001999.4(FBN2):c.1423G>A (p.Gly475Ser) rs200440156
NM_001999.4(FBN2):c.1435G>A (p.Gly479Arg) rs147346327
NM_001999.4(FBN2):c.1505C>G (p.Ala502Gly) rs369405711
NM_001999.4(FBN2):c.1526G>T (p.Arg509Leu) rs199587570
NM_001999.4(FBN2):c.1553G>A (p.Arg518Gln) rs748051713
NM_001999.4(FBN2):c.1651A>G (p.Asn551Asp) rs138389072
NM_001999.4(FBN2):c.1720A>G (p.Ile574Val) rs768073096
NM_001999.4(FBN2):c.1780A>G (p.Thr594Ala) rs1554064868
NM_001999.4(FBN2):c.1804del (p.Cys602fs) rs886038824
NM_001999.4(FBN2):c.1844G>T (p.Cys615Phe) rs1060503507
NM_001999.4(FBN2):c.1885A>G (p.Asn629Asp) rs863223554
NM_001999.4(FBN2):c.2042G>A (p.Arg681His) rs548605398
NM_001999.4(FBN2):c.2161G>C (p.Gly721Arg) rs149733159
NM_001999.4(FBN2):c.217C>A (p.Arg73Ser) rs148493036
NM_001999.4(FBN2):c.2365G>A (p.Gly789Ser) rs886038969
NM_001999.4(FBN2):c.244G>A (p.Val82Met) rs550387143
NM_001999.4(FBN2):c.2478C>G (p.Cys826Trp) rs1554125090
NM_001999.4(FBN2):c.2480G>A (p.Arg827Gln) rs150735582
NM_001999.4(FBN2):c.2536G>A (p.Glu846Lys) rs375666281
NM_001999.4(FBN2):c.2651G>C (p.Ser884Thr) rs139035999
NM_001999.4(FBN2):c.2722G>A (p.Glu908Lys) rs1204772554
NM_001999.4(FBN2):c.2777C>A (p.Ala926Asp) rs138429045
NM_001999.4(FBN2):c.2836G>T (p.Ala946Ser) rs886038950
NM_001999.4(FBN2):c.287_289del (p.Tyr96del) rs555068280
NM_001999.4(FBN2):c.2978G>A (p.Arg993His) rs774483323
NM_001999.4(FBN2):c.2996G>A (p.Arg999His) rs1342942240
NM_001999.4(FBN2):c.3039C>G (p.Ile1013Met) rs1388119592
NM_001999.4(FBN2):c.3114G>C (p.Glu1038Asp) rs199938409
NM_001999.4(FBN2):c.3296G>A (p.Arg1099His) rs202050092
NM_001999.4(FBN2):c.3394G>A (p.Val1132Ile) rs138834515
NM_001999.4(FBN2):c.3430G>A (p.Glu1144Lys) rs200060005
NM_001999.4(FBN2):c.3490C>T (p.Arg1164Cys) rs886039059
NM_001999.4(FBN2):c.362A>G (p.Asp121Gly) rs770483769
NM_001999.4(FBN2):c.3710G>T (p.Arg1237Leu) rs142185964
NM_001999.4(FBN2):c.3839C>T (p.Ser1280Leu) rs200481467
NM_001999.4(FBN2):c.3884A>G (p.Asp1295Gly) rs775987665
NM_001999.4(FBN2):c.3919C>T (p.Arg1307Cys) rs922751471
NM_001999.4(FBN2):c.3958A>G (p.Met1320Val) rs759481427
NM_001999.4(FBN2):c.4096A>G (p.Thr1366Ala) rs768722316
NM_001999.4(FBN2):c.4184G>T (p.Cys1395Phe) rs886038935
NM_001999.4(FBN2):c.4201G>A (p.Gly1401Arg) rs1554122552
NM_001999.4(FBN2):c.4258A>G (p.Ser1420Gly) rs1407868144
NM_001999.4(FBN2):c.4316G>A (p.Gly1439Asp) rs886039151
NM_001999.4(FBN2):c.4402G>A (p.Val1468Ile) rs199668238
NM_001999.4(FBN2):c.4495A>C (p.Asn1499His) rs771260299
NM_001999.4(FBN2):c.4559G>T (p.Gly1520Val) rs886038767
NM_001999.4(FBN2):c.460A>G (p.Met154Val) rs878854475
NM_001999.4(FBN2):c.4642G>A (p.Val1548Ile) rs140313460
NM_001999.4(FBN2):c.4724G>A (p.Arg1575His) rs776040052
NM_001999.4(FBN2):c.4757G>A (p.Arg1586Gln) rs143195229
NM_001999.4(FBN2):c.4757G>C (p.Arg1586Pro) rs143195229
NM_001999.4(FBN2):c.4763A>T (p.Asp1588Val) rs202218356
NM_001999.4(FBN2):c.4801G>A (p.Val1601Ile) rs762108847
NM_001999.4(FBN2):c.4829T>C (p.Leu1610Pro) rs886038891
NM_001999.4(FBN2):c.4864C>A (p.Pro1622Thr) rs750116860
NM_001999.4(FBN2):c.488A>G (p.His163Arg) rs1029299660
NM_001999.4(FBN2):c.4994A>G (p.Asn1665Ser) rs886038773
NM_001999.4(FBN2):c.5037A>C (p.Gln1679His) rs1554120349
NM_001999.4(FBN2):c.5275A>C (p.Lys1759Gln) rs201113098
NM_001999.4(FBN2):c.5531T>C (p.Leu1844Pro) rs755917639
NM_001999.4(FBN2):c.5762A>G (p.Asn1921Ser) rs1160016215
NM_001999.4(FBN2):c.5834A>G (p.Asn1945Ser) rs863223578
NM_001999.4(FBN2):c.6077C>T (p.Ser2026Phe) rs139668142
NM_001999.4(FBN2):c.6118A>G (p.Arg2040Gly) rs886038814
NM_001999.4(FBN2):c.6280C>T (p.Arg2094Trp) rs1262453464
NM_001999.4(FBN2):c.6445+5G>A rs761871037
NM_001999.4(FBN2):c.6681A>G (p.Thr2227=) rs145681607
NM_001999.4(FBN2):c.671T>C (p.Met224Thr) rs886038798
NM_001999.4(FBN2):c.672G>T (p.Met224Ile) rs371292311
NM_001999.4(FBN2):c.6764A>G (p.Asn2255Ser) rs886039147
NM_001999.4(FBN2):c.6805A>G (p.Met2269Val) rs943225631
NM_001999.4(FBN2):c.6833C>A (p.Thr2278Lys) rs2307109
NM_001999.4(FBN2):c.6898G>A (p.Glu2300Lys) rs1419124277
NM_001999.4(FBN2):c.68C>G (p.Ala23Gly) rs199560824
NM_001999.4(FBN2):c.6910G>A (p.Asp2304Asn) rs368802769
NM_001999.4(FBN2):c.6989G>A (p.Arg2330Lys) rs886038992
NM_001999.4(FBN2):c.7085G>C (p.Arg2362Thr) rs771718967
NM_001999.4(FBN2):c.7112C>G (p.Ser2371Ter) rs1461140915
NM_001999.4(FBN2):c.7195T>A (p.Ser2399Thr) rs1554117123
NM_001999.4(FBN2):c.7201A>C (p.Ser2401Arg) rs777558947
NM_001999.4(FBN2):c.7250G>T (p.Gly2417Val) rs886038938
NM_001999.4(FBN2):c.7418G>A (p.Arg2473Gln) rs28763925
NM_001999.4(FBN2):c.7496C>T (p.Pro2499Leu) rs199583859
NM_001999.4(FBN2):c.7511A>G (p.Tyr2504Cys) rs764032053
NM_001999.4(FBN2):c.7565T>C (p.Val2522Ala) rs886039005
NM_001999.4(FBN2):c.756G>T (p.Glu252Asp) rs565550310
NM_001999.4(FBN2):c.761G>C (p.Cys254Ser) rs755760127
NM_001999.4(FBN2):c.7796G>A (p.Cys2599Tyr) rs1554116599
NM_001999.4(FBN2):c.7841-3C>T rs1554116417
NM_001999.4(FBN2):c.7879G>A (p.Gly2627Ser) rs369568420
NM_001999.4(FBN2):c.787C>T (p.Arg263Trp) rs151329128
NM_001999.4(FBN2):c.7901G>A (p.Gly2634Asp) rs756511141
NM_001999.4(FBN2):c.7963G>A (p.Glu2655Lys) rs753526426
NM_001999.4(FBN2):c.7987G>A (p.Ala2663Thr) rs1245151549
NM_001999.4(FBN2):c.8035G>T (p.Ala2679Ser) rs763870762
NM_001999.4(FBN2):c.8082C>A (p.His2694Gln) rs142755118
NM_001999.4(FBN2):c.8119A>C (p.Asn2707His) rs886039073
NM_001999.4(FBN2):c.8193-4A>G rs200964477
NM_001999.4(FBN2):c.8239C>G (p.Leu2747Val) rs145353444
NM_001999.4(FBN2):c.8279A>C (p.Glu2760Ala) rs56023452
NM_001999.4(FBN2):c.8282C>T (p.Ala2761Val) rs201962592
NM_001999.4(FBN2):c.8498G>A (p.Arg2833His) rs753753954
NM_001999.4(FBN2):c.8513A>G (p.Gln2838Arg) rs772928933
NM_001999.4(FBN2):c.8597G>T (p.Gly2866Val) rs886038818

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.