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rs10226084

From SNPedia

Orientationplus
Stabilizedplus
Make rs10226084(C;C)
Make rs10226084(C;T)
Make rs10226084(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position17957989
is asnp
is mentioned by
dbSNPrs10226084
ebirs10226084
HLIrs10226084
Exacrs10226084
Varsomers10226084
Maprs10226084
PheGenIrs10226084
hapmaprs10226084
1000 genomesrs10226084
hgdprs10226084
ensemblrs10226084
gopubmedrs10226084
geneviewrs10226084
scholarrs10226084
googlers10226084
pharmgkbrs10226084
gwascentralrs10226084
openSNPrs10226084
23andMers10226084
23andMe allrs10226084
SNP Nexus

SNPshotrs10226084
SNPdbers10226084
MSV3drs10226084
GWAS Ctlgrs10226084
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 T
P-val 5E-10
Odds Ratio .01 [0.005-0.009] unit decrease