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

rs164390

From SNPedia

Orientationplus
Stabilizedplus
Make rs164390(G;G)
Make rs164390(G;T)
Make rs164390(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position69167187
GeneCCNB1
is asnp
is mentioned by
dbSNPrs164390
ebirs164390
HLIrs164390
Exacrs164390
Varsomers164390
Maprs164390
PheGenIrs164390
hapmaprs164390
1000 genomesrs164390
hgdprs164390
ensemblrs164390
gopubmedrs164390
geneviewrs164390
scholarrs164390
googlers164390
pharmgkbrs164390
gwascentralrs164390
openSNPrs164390
23andMers164390
23andMe allrs164390
SNP Nexus

SNPshotrs164390
SNPdbers164390
MSV3drs164390
GWAS Ctlgrs164390
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 24395923] Genetic variants in CCNB1 associated with differential gene transcription and risk of coronary in-stent restenosis