ClinVar Miner

List of variants reported as uncertain significance for congenital fibrinogen deficiency

Included ClinVar conditions (10):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 130
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HGVS dbSNP gnomAD frequency
NM_021870.3(FGG):c.*488C>T rs191297318 0.00453
NM_021870.3(FGG):c.571G>A (p.Gly191Arg) rs6063 0.00339
NM_005141.5(FGB):c.794C>T (p.Pro265Leu) rs6054 0.00275
NM_021870.3(FGG):c.*496A>C rs187316301 0.00268
NM_005141.5(FGB):c.*846T>G rs541828079 0.00166
NM_005141.5(FGB):c.*233G>T rs539731011 0.00154
NM_005141.5(FGB):c.298C>T (p.Pro100Ser) rs2227434 0.00134
NM_021870.3(FGG):c.*500C>T rs183036893 0.00103
NM_005141.5(FGB):c.115-12C>T rs187641148 0.00058
NM_005141.5(FGB):c.*450T>A rs183181144 0.00053
NM_021870.3(FGG):c.140C>T (p.Thr47Ile) rs138511699 0.00050
NM_021871.4(FGA):c.1417G>A (p.Asp473Asn) rs200378626 0.00048
NM_005141.5(FGB):c.1244+7G>A rs142937995 0.00038
NM_005141.5(FGB):c.*624C>T rs754198978 0.00034
NM_021870.3(FGG):c.124G>A (p.Gly42Ser) rs202132393 0.00034
NM_005141.5(FGB):c.*1671C>T rs765773409 0.00032
NM_021871.4(FGA):c.244A>C (p.Thr82Pro) rs199554805 0.00031
NM_005141.5(FGB):c.*1771C>T rs776780011 0.00026
NM_005141.5(FGB):c.*592G>A rs376470048 0.00019
NM_021871.4(FGA):c.616C>G (p.Gln206Glu) rs560732073 0.00019
NM_021870.3(FGG):c.318C>T (p.Asp106=) rs150242757 0.00016
NM_021870.3(FGG):c.1258A>G (p.Ile420Val) rs374917187 0.00015
NM_005141.5(FGB):c.*1687A>G rs992721102 0.00014
NM_005141.5(FGB):c.*1738G>A rs760784701 0.00014
NM_005141.5(FGB):c.*363A>G rs545671394 0.00013
NM_005141.5(FGB):c.*1105A>G rs542187592 0.00012
NM_005141.5(FGB):c.200G>C (p.Ser67Thr) rs371842822 0.00011
NM_021871.4(FGA):c.*50T>G rs369606098 0.00010
NM_005141.5(FGB):c.*1372T>A rs371670019 0.00009
NM_021870.3(FGG):c.620A>G (p.Tyr207Cys) rs775086103 0.00008
NM_021871.4(FGA):c.1072G>A (p.Gly358Arg) rs201105899 0.00007
NM_000509.5(FGG):c.-130G>T rs749800940 0.00006
NM_005141.5(FGB):c.*1444C>A rs886059145 0.00006
NM_021870.3(FGG):c.19C>T (p.Pro7Ser) rs374845868 0.00006
NM_021871.4(FGA):c.1823G>C (p.Gly608Ala) rs370873387 0.00006
NM_005141.5(FGB):c.*304G>A rs901759260 0.00005
NM_021870.3(FGG):c.709T>C (p.Tyr237His) rs762488338 0.00005
NM_000204.5(CFI):c.1532C>T (p.Ala511Val) rs760801046 0.00004
NM_005141.5(FGB):c.752C>T (p.Thr251Ile) rs776988939 0.00004
NM_021871.4(FGA):c.1838A>G (p.His613Arg) rs201686865 0.00004
NM_021871.4(FGA):c.765G>A (p.Pro255=) rs779582722 0.00004
NM_021871.4(FGA):c.923G>A (p.Arg308Gln) rs760992799 0.00004
NM_005141.5(FGB):c.*1542T>C rs886059146 0.00003
NM_005141.5(FGB):c.*15A>G rs375561591 0.00003
NM_005141.5(FGB):c.*1867T>C rs886059148 0.00003
NM_005141.5(FGB):c.*303C>T rs886059142 0.00003
NM_005141.5(FGB):c.4A>G (p.Lys2Glu) rs6053 0.00003
NM_005141.5(FGB):c.749A>G (p.Glu250Gly) rs759800033 0.00003
NM_021870.3(FGG):c.1285G>T (p.Gly429Trp) rs145938787 0.00003
NM_021871.4(FGA):c.1718G>A (p.Arg573His) rs78506343 0.00003
NM_005141.5(FGB):c.*464C>T rs940820346 0.00002
NM_005141.5(FGB):c.*526C>T rs933339992 0.00002
NM_005141.5(FGB):c.251A>C (p.Lys84Thr) rs886059141 0.00002
NM_021870.3(FGG):c.683T>C (p.Val228Ala) rs757702704 0.00002
NM_021871.4(FGA):c.1918C>G (p.Pro640Ala) rs199571440 0.00002
NM_021871.4(FGA):c.450G>A (p.Gln150=) rs368446857 0.00002
NM_021871.4(FGA):c.8C>T (p.Ser3Phe) rs771156473 0.00002
NM_000508.5(FGA):c.2527T>C (p.Trp843Arg) rs1280924091 0.00001
NM_005141.5(FGB):c.*1019G>T rs1478189415 0.00001
NM_005141.5(FGB):c.*1892G>A rs765456260 0.00001
NM_005141.5(FGB):c.*36A>G rs758231685 0.00001
NM_005141.5(FGB):c.*427G>A rs1196345013 0.00001
NM_005141.5(FGB):c.-6_-5del rs757727864 0.00001
NM_005141.5(FGB):c.103G>A (p.Asp35Asn) rs747783086 0.00001
NM_005141.5(FGB):c.332A>G (p.Gln111Arg) rs758080375 0.00001
NM_005141.5(FGB):c.564T>C (p.Asn188=) rs759250713 0.00001
NM_005141.5(FGB):c.656A>G (p.Gln219Arg) rs778766319 0.00001
NM_005141.5(FGB):c.659T>C (p.Met220Thr) rs1363577874 0.00001
NM_005141.5(FGB):c.762G>A (p.Met254Ile) rs201536638 0.00001
NM_005141.5(FGB):c.80T>C (p.Leu27Pro) rs1442627097 0.00001
NM_021870.3(FGG):c.*494A>G rs1731056413 0.00001
NM_021870.3(FGG):c.1125C>T (p.Tyr375=) rs766524002 0.00001
NM_021870.3(FGG):c.502A>G (p.Thr168Ala) rs141559764 0.00001
NM_021870.3(FGG):c.667-10G>C rs886059155 0.00001
NM_021871.4(FGA):c.1025G>A (p.Gly342Glu) rs774664670 0.00001
NM_021871.4(FGA):c.1463G>A (p.Gly488Asp) rs1382669489 0.00001
NM_021871.4(FGA):c.1470C>G (p.Asp490Glu) rs1335171406 0.00001
NM_021871.4(FGA):c.1912G>A (p.Gly638Arg) rs771429165 0.00001
NM_021871.4(FGA):c.1915A>G (p.Lys639Glu) rs1424019951 0.00001
NM_021871.4(FGA):c.346G>A (p.Asp116Asn) rs886059153 0.00001
NM_021871.4(FGA):c.822C>T (p.Ser274=) rs886059150 0.00001
NM_021871.4(FGA):c.919A>G (p.Asn307Asp) rs750564329 0.00001
NM_000508.5(FGA):c.2021T>C (p.Leu674Ser) rs2110806407
NM_000508.5(FGA):c.2024T>C (p.Ile675Thr) rs2110806390
NM_000508.5(FGA):c.2024T>G (p.Ile675Ser) rs2110806390
NM_000508.5(FGA):c.2128G>A (p.Gly710Ser) rs2110806103
NM_000508.5(FGA):c.2350C>T (p.Gln784Ter) rs148824832
NM_000508.5(FGA):c.2372A>T (p.Asp791Val) rs1479874554
NM_000509.5(FGG):c.-53A>G rs886059156
NM_005141.5(FGB):c.*1204T>C rs1447745807
NM_005141.5(FGB):c.*1252A>C rs1730444171
NM_005141.5(FGB):c.*1409C>A rs886059144
NM_005141.5(FGB):c.*1544T>C rs886059147
NM_005141.5(FGB):c.*1639T>C rs1026178982
NM_005141.5(FGB):c.*1998A>G rs886059149
NM_005141.5(FGB):c.*277A>G rs1466304617
NM_005141.5(FGB):c.*361A>T rs886059143
NM_005141.5(FGB):c.*496G>A rs557290052
NM_005141.5(FGB):c.*801A>G rs1578787077
NM_005141.5(FGB):c.*835del rs768727295
NM_005141.5(FGB):c.114+11del rs779228767
NM_005141.5(FGB):c.1292G>T (p.Gly431Val) rs779328318
NM_005141.5(FGB):c.1330G>A (p.Gly444Ser)
NM_005141.5(FGB):c.169C>T (p.Pro57Ser) rs971404907
NM_005141.5(FGB):c.210C>T (p.Gly70=) rs933834957
NM_005141.5(FGB):c.254T>C (p.Val85Ala) rs775809959
NM_005141.5(FGB):c.284G>A (p.Cys95Tyr) rs2110761933
NM_005141.5(FGB):c.419C>A (p.Thr140Asn)
NM_005141.5(FGB):c.506T>A (p.Val169Asp) rs2110768107
NM_005141.5(FGB):c.691T>C (p.Cys231Arg) rs1730226269
NM_005141.5(FGB):c.811G>T (p.Asp271Tyr) rs913936601
NM_005141.5(FGB):c.946T>C (p.Cys316Arg)
NM_021870.3(FGG):c.1190C>T (p.Thr397Ile) rs1731071910
NM_021870.3(FGG):c.1202G>A (p.Arg401Gln) rs2110838894
NM_021870.3(FGG):c.1237A>G (p.Ile413Val) rs886059154
NM_021870.3(FGG):c.1300G>T (p.Val434Phe)
NM_021870.3(FGG):c.401G>A (p.Arg134Gln) rs764559342
NM_021870.3(FGG):c.606G>C (p.Gln202His) rs2110846559
NM_021870.3(FGG):c.694A>G (p.Lys232Glu) rs2110844685
NM_021870.3(FGG):c.700T>C (p.Trp234Arg) rs2110844651
NM_021870.3(FGG):c.793C>T (p.Gln265Ter) rs771279321
NM_021871.4(FGA):c.*133G>A rs182736373
NM_021871.4(FGA):c.103C>G (p.Arg35Gly) rs121909606
NM_021871.4(FGA):c.1207G>A (p.Ala403Thr) rs1730710209
NM_021871.4(FGA):c.1486G>T (p.Asp496Tyr) rs2110809573
NM_021871.4(FGA):c.1930C>G (p.Pro644Ala) rs1730682953
NM_021871.4(FGA):c.364+5G>A rs891744509
NM_021871.4(FGA):c.614A>G (p.Glu205Gly) rs886059152
NM_021871.4(FGA):c.666A>T (p.Pro222=) rs886059151
NM_021871.4(FGA):c.829T>C (p.Tyr277His) rs1473392017

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