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rs4681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs4681(C;T)
Make rs4681(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154569680
GeneFGB
is asnp
is mentioned by
dbSNPrs4681
dbSNP (old)rs4681
ClinGenrs4681
ebirs4681
HLIrs4681
Exacrs4681
Gnomadrs4681
Varsomers4681
Maprs4681
PheGenIrs4681
Biobankrs4681
1000 genomesrs4681
hgdprs4681
ensemblrs4681
gopubmedrs4681
geneviewrs4681
scholarrs4681
googlers4681
pharmgkbrs4681
gwascentralrs4681
openSNPrs4681
23andMers4681
23andMe allrs4681
SNP Nexus

SNPshotrs4681
SNPdbers4681
MSV3drs4681
GWAS Ctlgrs4681
GMAF0.1556
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20167083OA-icon.png] Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study


ClinVar
Risk rs4681(T;T)
Alt rs4681(T;T)
Reference Rs4681(C;C)
Significance Probable-non-pathogenic
Disease not specified Afibrinogenemia
Variation info
Gene FGB
CLNDBN not specified Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155490832C>T
CLNSRC
CLNACC RCV000247915.1, RCV000339658.1,