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rs4817986

From SNPedia

Orientationplus
Stabilizedplus
Make rs4817986(G;G)
Make rs4817986(G;T)
Make rs4817986(T;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position39093586
is asnp
is mentioned by
dbSNPrs4817986
ebirs4817986
HLIrs4817986
Exacrs4817986
Varsomers4817986
Maprs4817986
PheGenIrs4817986
hapmaprs4817986
1000 genomesrs4817986
hgdprs4817986
ensemblrs4817986
gopubmedrs4817986
geneviewrs4817986
scholarrs4817986
googlers4817986
pharmgkbrs4817986
gwascentralrs4817986
openSNPrs4817986
23andMers4817986
23andMe allrs4817986
SNP Nexus

SNPshotrs4817986
SNPdbers4817986
MSV3drs4817986
GWAS Ctlgrs4817986
Max Magnitude
? (G;G) (G;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 2E-11
Odds Ratio .01 [0.006-0.01] unit decrease