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rs121913093

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913093(G;T)
Make rs121913093(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154606768
GeneFGG
is asnp
is mentioned by
dbSNPrs121913093
ebirs121913093
HLIrs121913093
Exacrs121913093
Varsomers121913093
Maprs121913093
PheGenIrs121913093
hapmaprs121913093
1000 genomesrs121913093
hgdprs121913093
ensemblrs121913093
gopubmedrs121913093
geneviewrs121913093
scholarrs121913093
googlers121913093
pharmgkbrs121913093
gwascentralrs121913093
openSNPrs121913093
23andMers121913093
23andMe allrs121913093
SNP Nexus

SNPshotrs121913093
SNPdbers121913093
MSV3drs121913093
GWAS Ctlgrs121913093
Max Magnitude0
OMIM134850
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121913093(T;T)
Alt rs121913093(T;T)
Reference rs121913093(G;G)
Significance Other
Disease FIBRINOGEN KYOTO 3
Variation info
Gene FGG
CLNDBN FIBRINOGEN KYOTO 3
Reversed 1
HGVS NC_000004.11:g.155527920C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017789.1,