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rs121913089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913089(G;T)
Make rs121913089(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154606881
GeneFGG
is asnp
is mentioned by
dbSNPrs121913089
ebirs121913089
HLIrs121913089
Exacrs121913089
Varsomers121913089
Maprs121913089
PheGenIrs121913089
hapmaprs121913089
1000 genomesrs121913089
hgdprs121913089
ensemblrs121913089
gopubmedrs121913089
geneviewrs121913089
scholarrs121913089
googlers121913089
pharmgkbrs121913089
gwascentralrs121913089
openSNPrs121913089
23andMers121913089
23andMe allrs121913089
SNP Nexus

SNPshotrs121913089
SNPdbers121913089
MSV3drs121913089
GWAS Ctlgrs121913089
Max Magnitude0
OMIM134850
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913089(T;T)
Alt rs121913089(T;T)
Reference rs121913089(G;G)
Significance Other
Disease FIBRINOGEN BALTIMORE 1
Variation info
Gene FGG
CLNDBN FIBRINOGEN BALTIMORE 1
Reversed 1
HGVS NC_000004.11:g.155528033C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017783.3,