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rs1476698

From SNPedia

Orientationminus
Stabilizedminus
Make rs1476698(C;C)
Make rs1476698(C;T)
Make rs1476698(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position241357034
GeneFARP2
is asnp
is mentioned by
dbSNPrs1476698
ebirs1476698
HLIrs1476698
Exacrs1476698
Varsomers1476698
Maprs1476698
PheGenIrs1476698
hapmaprs1476698
1000 genomesrs1476698
hgdprs1476698
ensemblrs1476698
gopubmedrs1476698
geneviewrs1476698
scholarrs1476698
googlers1476698
pharmgkbrs1476698
gwascentralrs1476698
openSNPrs1476698
23andMers1476698
23andMe allrs1476698
SNP Nexus

SNPshotrs1476698
SNPdbers1476698
MSV3drs1476698
GWAS Ctlgrs1476698
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23969696OA-icon.png]
Trait Fibrinogen
Title Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Risk Allele A
P-val 2E-9
Odds Ratio .01 [0.005-0.009] unit increase