rs164390
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs164390(G;G) |
Make rs164390(G;T) |
Make rs164390(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 69167187 |
Gene | CCNB1 |
is a | snp |
is | mentioned by |
dbSNP | rs164390 |
dbSNP (classic) | rs164390 |
ClinGen | rs164390 |
ebi | rs164390 |
HLI | rs164390 |
Exac | rs164390 |
Gnomad | rs164390 |
Varsome | rs164390 |
LitVar | rs164390 |
Map | rs164390 |
PheGenI | rs164390 |
Biobank | rs164390 |
1000 genomes | rs164390 |
hgdp | rs164390 |
ensembl | rs164390 |
geneview | rs164390 |
scholar | rs164390 |
rs164390 | |
pharmgkb | rs164390 |
gwascentral | rs164390 |
openSNP | rs164390 |
23andMe | rs164390 |
SNPshot | rs164390 |
SNPdbe | rs164390 |
MSV3d | rs164390 |
GWAS Ctlg | rs164390 |
Max Magnitude | 0 |
? | (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