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rs7681423

From SNPedia

Orientationplus
Stabilizedplus
Make rs7681423(C;C)
Make rs7681423(C;T)
Make rs7681423(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154621096
is asnp
is mentioned by
dbSNPrs7681423
ebirs7681423
HLIrs7681423
Exacrs7681423
Varsomers7681423
Maprs7681423
PheGenIrs7681423
hapmaprs7681423
1000 genomesrs7681423
hgdprs7681423
ensemblrs7681423
gopubmedrs7681423
geneviewrs7681423
scholarrs7681423
googlers7681423
pharmgkbrs7681423
gwascentralrs7681423
openSNPrs7681423
23andMers7681423
23andMe allrs7681423
SNP Nexus

SNPshotrs7681423
SNPdbers7681423
MSV3drs7681423
GWAS Ctlgrs7681423
GMAF0.3177
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21757653OA-icon.png]
Trait
Title Association of {gamma}' Fibrinogen With Cardiovascular Disease.
Risk Allele T
P-val 1E-109
Odds Ratio 0.2900 [0.26-0.32] g/L decrease