rs4147064
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4147064(C;C) |
Make rs4147064(C;T) |
Make rs4147064(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 13 |
Position | 30745981 |
Gene | ALOX5AP |
is a | snp |
is | mentioned by |
dbSNP | rs4147064 |
dbSNP (classic) | rs4147064 |
ClinGen | rs4147064 |
ebi | rs4147064 |
HLI | rs4147064 |
Exac | rs4147064 |
Gnomad | rs4147064 |
Varsome | rs4147064 |
LitVar | rs4147064 |
Map | rs4147064 |
PheGenI | rs4147064 |
Biobank | rs4147064 |
1000 genomes | rs4147064 |
hgdp | rs4147064 |
ensembl | rs4147064 |
geneview | rs4147064 |
scholar | rs4147064 |
rs4147064 | |
pharmgkb | rs4147064 |
gwascentral | rs4147064 |
openSNP | rs4147064 |
23andMe | rs4147064 |
SNPshot | rs4147064 |
SNPdbe | rs4147064 |
MSV3d | rs4147064 |
GWAS Ctlg | rs4147064 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26885075] A tagging ALOX5AP polymorphism and risk of ischemic stroke in a northeastern Chinese Han population.