ClinVar Miner

List of variants in gene FGG studied for coagulation protein disease

Included ClinVar conditions (69):
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Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_000509.5(FGG):c.*216C>T rs2066865 0.26358
NM_021870.3(FGG):c.418T>C (p.Tyr140His) rs2066870 0.01852
FIBRINOGEN PARIS 1 rs2066862 0.00546
NM_021870.3(FGG):c.*488C>T rs191297318 0.00453
NM_021870.3(FGG):c.78+9G>A rs2066857 0.00345
NM_021870.3(FGG):c.571G>A (p.Gly191Arg) rs6063 0.00339
NM_021870.3(FGG):c.*496A>C rs187316301 0.00268
NM_021870.3(FGG):c.323C>G (p.Ala108Gly) rs148685782 0.00222
NM_021870.3(FGG):c.*535A>G rs146143405 0.00140
NM_021870.3(FGG):c.*500C>T rs183036893 0.00103
NM_021870.3(FGG):c.140C>T (p.Thr47Ile) rs138511699 0.00050
NM_021870.3(FGG):c.124G>A (p.Gly42Ser) rs202132393 0.00034
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_021870.3(FGG):c.274C>T (p.Leu92Phe) rs142286849 0.00009
NM_021870.3(FGG):c.620A>G (p.Tyr207Cys) rs775086103 0.00008
NM_021870.3(FGG):c.19C>T (p.Pro7Ser) rs374845868 0.00006
NM_021870.3(FGG):c.709T>C (p.Tyr237His) rs762488338 0.00005
NM_021870.3(FGG):c.1099G>A (p.Ala367Thr) rs78257946 0.00004
NM_021870.3(FGG):c.1285G>T (p.Gly429Trp) rs145938787 0.00003
NM_021870.3(FGG):c.309T>C (p.Asn103=) rs138916334 0.00002
NM_021870.3(FGG):c.683T>C (p.Val228Ala) rs757702704 0.00002
NM_021870.2(FGG):c.902G>A (p.Arg301His) rs121913088 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_021870.3(FGG):c.677G>T (p.Gly226Val) rs1310452604 0.00001
NC_000004.11:g.(?_155525322)_(155533809_?)del
NM_000509.5(FGG):c.-53A>G rs886059156
NM_021870.2(FGG):c.1007T>C (p.Met336Thr) rs121913091
NM_021870.2(FGG):c.901C>T (p.Arg301Cys) rs121913087
NM_021870.3(FGG):c.1022G>A (p.Trp341Ter) rs1553965519
NM_021870.3(FGG):c.1030G>C (p.Asp344His)
NM_021870.3(FGG):c.1067A>G (p.Asp356Gly)
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.1210T>C (p.Ser404Pro) rs587777720
NM_021870.3(FGG):c.1237A>G (p.Ile413Val) rs886059154
NM_021870.3(FGG):c.1300G>T (p.Val434Phe)
NM_021870.3(FGG):c.207_208dup (p.Glu70fs) rs2110850824
NM_021870.3(FGG):c.307+5G>A rs587776838
NM_021870.3(FGG):c.331A>T (p.Lys111Ter) rs1578812509
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.666+23T>A rs1578810856
NM_021870.3(FGG):c.667-320A>T rs587776839
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.78+5G>A rs587776837
NM_021870.3(FGG):c.793C>T (p.Gln265Ter) rs771279321

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