ClinVar Miner

List of variants in gene FBN2 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_001999.4(FBN2):c.*234T>C
NM_001999.4(FBN2):c.*371T>G rs531108136
NM_001999.4(FBN2):c.*372del rs544546746
NM_001999.4(FBN2):c.*93_*95TAA[2] rs199925656
NM_001999.4(FBN2):c.-344G>C rs564044015
NM_001999.4(FBN2):c.-448C>T rs529025715
NM_001999.4(FBN2):c.1157T>C (p.Met386Thr)
NM_001999.4(FBN2):c.1435G>A (p.Gly479Arg) rs147346327
NM_001999.4(FBN2):c.1821A>G (p.Glu607=)
NM_001999.4(FBN2):c.2249-12T>C rs776314725
NM_001999.4(FBN2):c.2260G>A (p.Gly754Ser) rs145259927
NM_001999.4(FBN2):c.2536G>A (p.Glu846Lys) rs375666281
NM_001999.4(FBN2):c.2717G>A (p.Arg906His) rs370973542
NM_001999.4(FBN2):c.2874G>A (p.Glu958=) rs765859878
NM_001999.4(FBN2):c.3093G>A (p.Ala1031=)
NM_001999.4(FBN2):c.3217+13G>A rs572013507
NM_001999.4(FBN2):c.3296G>A (p.Arg1099His) rs202050092
NM_001999.4(FBN2):c.3480C>T (p.Asp1160=) rs142323824
NM_001999.4(FBN2):c.3518C>G (p.Thr1173Ser) rs199678757
NM_001999.4(FBN2):c.4035G>A (p.Lys1345=)
NM_001999.4(FBN2):c.4298G>A (p.Arg1433His) rs143462011
NM_001999.4(FBN2):c.4454A>G (p.Asp1485Gly) rs199665922
NM_001999.4(FBN2):c.4642G>A (p.Val1548Ile) rs140313460
NM_001999.4(FBN2):c.4801G>A (p.Val1601Ile) rs762108847
NM_001999.4(FBN2):c.4902C>T (p.Pro1634=) rs201071253
NM_001999.4(FBN2):c.532C>T (p.Pro178Ser) rs765177174
NM_001999.4(FBN2):c.5447C>T (p.Pro1816Leu) rs149537608
NM_001999.4(FBN2):c.5487C>T (p.Gly1829=) rs375136629
NM_001999.4(FBN2):c.5674+7A>G rs367877964
NM_001999.4(FBN2):c.5917+9T>G rs371439173
NM_001999.4(FBN2):c.6253C>G (p.Pro2085Ala) rs34845843
NM_001999.4(FBN2):c.6437A>G (p.Asp2146Gly)
NM_001999.4(FBN2):c.6666G>A (p.Pro2222=) rs192923239
NM_001999.4(FBN2):c.68C>G (p.Ala23Gly) rs199560824
NM_001999.4(FBN2):c.6946A>T (p.Ile2316Phe) rs201220519
NM_001999.4(FBN2):c.7012+7G>A rs199735209
NM_001999.4(FBN2):c.7418G>T (p.Arg2473Leu) rs28763925
NM_001999.4(FBN2):c.76A>G (p.Thr26Ala) rs374922166
NM_001999.4(FBN2):c.7878C>T (p.His2626=) rs587780943
NM_001999.4(FBN2):c.8082C>A (p.His2694Gln) rs142755118
NM_001999.4(FBN2):c.8257G>A (p.Glu2753Lys) rs146781484
NM_001999.4(FBN2):c.8282C>T (p.Ala2761Val) rs201962592
NM_001999.4(FBN2):c.8376C>G (p.Ile2792Met) rs142747169
NM_001999.4(FBN2):c.8574G>A (p.Thr2858=) rs573245869
NM_001999.4(FBN2):c.976C>T (p.Pro326Ser) rs28763954

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