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rs2227389

From SNPedia

Orientationplus
Stabilizedplus
Make rs2227389(C;C)
Make rs2227389(C;T)
Make rs2227389(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position154562018
GeneFGB
is asnp
is mentioned by
dbSNPrs2227389
ebirs2227389
HLIrs2227389
Exacrs2227389
Varsomers2227389
Maprs2227389
PheGenIrs2227389
hapmaprs2227389
1000 genomesrs2227389
hgdprs2227389
ensemblrs2227389
gopubmedrs2227389
geneviewrs2227389
scholarrs2227389
googlers2227389
pharmgkbrs2227389
gwascentralrs2227389
openSNPrs2227389
23andMers2227389
23andMe allrs2227389
SNP Nexus

SNPshotrs2227389
SNPdbers2227389
MSV3drs2227389
GWAS Ctlgrs2227389
Max Magnitude

[PMID 26054681] Association of seven thrombotic pathway gene CpG-SNPs with coronary heart disease