Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913087

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913087(C;T)
Make rs121913087(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154606933
GeneFGG
is asnp
is mentioned by
dbSNPrs121913087
ClinGenrs121913087
ebirs121913087
HLIrs121913087
Exacrs121913087
Varsomers121913087
Maprs121913087
PheGenIrs121913087
hapmaprs121913087
1000 genomesrs121913087
hgdprs121913087
ensemblrs121913087
gopubmedrs121913087
geneviewrs121913087
scholarrs121913087
googlers121913087
pharmgkbrs121913087
gwascentralrs121913087
openSNPrs121913087
23andMers121913087
23andMe allrs121913087
SNP Nexus

SNPshotrs121913087
SNPdbers121913087
MSV3drs121913087
GWAS Ctlgrs121913087
Max Magnitude0
OMIM134850
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913087(T;T)
Alt rs121913087(T;T)
Reference Rs121913087(C;C)
Significance Other
Disease FIBRINOGEN TOKYO 2
Variation info
Gene FGG
CLNDBN FIBRINOGEN TOKYO 2
Reversed 1
HGVS NC_000004.11:g.155528085G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000017772.5,