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

rs434943

From SNPedia

Orientationminus
Stabilizedminus
Make rs434943(C;C)
Make rs434943(C;T)
Make rs434943(T;T)
ReferenceGRCh38 38.1/142
Chromosome14
Position68847342
is asnp
is mentioned by
dbSNPrs434943
ebirs434943
HLIrs434943
Exacrs434943
Varsomers434943
Maprs434943
PheGenIrs434943
hapmaprs434943
1000 genomesrs434943
hgdprs434943
ensemblrs434943
gopubmedrs434943
geneviewrs434943
scholarrs434943
googlers434943
pharmgkbrs434943
gwascentralrs434943
openSNPrs434943
23andMers434943
23andMe allrs434943
SNP Nexus

SNPshotrs434943
SNPdbers434943
MSV3drs434943
GWAS Ctlgrs434943
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 1E-8
Odds Ratio .01 [0.005-0.009] unit increase