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

rs7673587

From SNPedia

Orientationplus
Stabilizedplus
Make rs7673587(C;C)
Make rs7673587(C;T)
Make rs7673587(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154559282
is asnp
is mentioned by
dbSNPrs7673587
ebirs7673587
HLIrs7673587
Exacrs7673587
Varsomers7673587
Maprs7673587
PheGenIrs7673587
hapmaprs7673587
1000 genomesrs7673587
hgdprs7673587
ensemblrs7673587
gopubmedrs7673587
geneviewrs7673587
scholarrs7673587
googlers7673587
pharmgkbrs7673587
gwascentralrs7673587
openSNPrs7673587
23andMers7673587
23andMe allrs7673587
SNP Nexus

SNPshotrs7673587
SNPdbers7673587
MSV3drs7673587
GWAS Ctlgrs7673587
GMAF0.1887
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20167083OA-icon.png] Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study