ClinVar Miner

List of variants in gene FGG studied for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
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.709T>C (p.Tyr237His) rs762488338 0.00005
NM_021870.3(FGG):c.1099G>A (p.Ala367Thr) rs78257946 0.00004
NM_021870.3(FGG):c.19C>T (p.Pro7Ser) rs374845868 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.1006A>T (p.Met336Leu)
NM_021870.3(FGG):c.1022G>A (p.Trp341Ter) rs1553965519
NM_021870.3(FGG):c.1030G>C (p.Asp344His)
NM_021870.3(FGG):c.1037A>G (p.Asp346Gly)
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.124-2A>G
NM_021870.3(FGG):c.1242del (p.Phe415fs)
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.702G>T (p.Trp234Cys)
NM_021870.3(FGG):c.78+5G>A rs587776837
NM_021870.3(FGG):c.793C>T (p.Gln265Ter) rs771279321

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.