ClinVar Miner

List of variants in gene FBLN5 reported as uncertain significance for age-related macular degeneration

Included ClinVar conditions (40):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_006329.4(FBLN5):c.*648G>A rs182435130 0.00140
NM_006329.4(FBLN5):c.*363C>T rs536827304 0.00049
NM_006329.4(FBLN5):c.*121C>T rs548351890 0.00033
NM_006329.4(FBLN5):c.143C>T (p.Thr48Ile) rs141200859 0.00026
NM_006329.4(FBLN5):c.799G>A (p.Gly267Ser) rs149396611 0.00026
NM_006329.4(FBLN5):c.989+9C>T rs557362799 0.00026
NM_006329.4(FBLN5):c.862+12C>T rs202088447 0.00025
NM_006329.4(FBLN5):c.1241G>A (p.Arg414Gln) rs142907552 0.00019
NM_006329.4(FBLN5):c.268G>A (p.Gly90Ser) rs144288844 0.00019
NM_006329.4(FBLN5):c.1191G>A (p.Thr397=) rs148660796 0.00014
NM_006329.4(FBLN5):c.1051C>T (p.Arg351Trp) rs28939073 0.00010
NM_006329.4(FBLN5):c.*98G>A rs568348723 0.00009
NM_006329.4(FBLN5):c.*426C>T rs553193064 0.00008
NM_006329.4(FBLN5):c.-413C>T rs886050892 0.00007
NM_006329.4(FBLN5):c.901C>A (p.Leu301Met) rs377360782 0.00005
NM_006329.4(FBLN5):c.1087G>A (p.Ala363Thr) rs121434302 0.00004
NM_006329.4(FBLN5):c.273G>A (p.Pro91=) rs368771780 0.00004
NM_006329.4(FBLN5):c.*458T>C rs886050887 0.00003
NM_006329.4(FBLN5):c.178G>C (p.Val60Leu) rs121434299 0.00002
NM_006329.4(FBLN5):c.212G>A (p.Arg71Gln) rs121434300 0.00002
NM_006329.4(FBLN5):c.*419G>C rs1451509746 0.00001
NM_006329.4(FBLN5):c.*653G>A rs886050886 0.00001
NM_006329.4(FBLN5):c.*775A>C rs886050885 0.00001
NM_006329.4(FBLN5):c.*77T>A rs1326922015 0.00001
NM_006329.4(FBLN5):c.-382C>G rs886050890 0.00001
NM_006329.4(FBLN5):c.1183C>T (p.Arg395Trp) rs372650987 0.00001
NM_006329.4(FBLN5):c.245A>C (p.Asn82Thr) rs759508064 0.00001
NM_006329.4(FBLN5):c.251A>G (p.Tyr84Cys) rs886050889 0.00001
NM_006329.4(FBLN5):c.336A>G (p.Ile112Met) rs1221579102 0.00001
NM_006329.4(FBLN5):c.573A>G (p.Thr191=) rs756288143 0.00001
NM_006329.4(FBLN5):c.676G>A (p.Gly226Ser) rs747288805 0.00001
NM_006329.4(FBLN5):c.-139C>T rs554315938
NM_006329.4(FBLN5):c.-389C>A rs886050891
NM_006329.4(FBLN5):c.-428G>C rs886050893
NM_006329.4(FBLN5):c.-77C>G rs751344551
NM_006329.4(FBLN5):c.1063G>C (p.Val355Leu) rs754104809
NM_006329.4(FBLN5):c.1235G>A (p.Gly412Glu) rs121434303
NM_006329.4(FBLN5):c.124+8C>A rs2056089374
NM_006329.4(FBLN5):c.259C>T (p.Pro87Ser) rs121434301
NM_006329.4(FBLN5):c.371A>C (p.Gln124Pro)
NM_006329.4(FBLN5):c.388G>A (p.Glu130Lys) rs886050888
NM_006329.4(FBLN5):c.506T>C (p.Ile169Thr) rs28939072
NM_006329.4(FBLN5):c.726C>G (p.Gly242=) rs148209555
NM_006329.4(FBLN5):c.992G>A (p.Arg331His) rs774735234

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