rs25651
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs25651(A;A) |
Make rs25651(A;G) |
Make rs25651(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 89792557 |
Gene | ANPEP |
is a | snp |
is | mentioned by |
dbSNP | rs25651 |
dbSNP (classic) | rs25651 |
ClinGen | rs25651 |
ebi | rs25651 |
HLI | rs25651 |
Exac | rs25651 |
Gnomad | rs25651 |
Varsome | rs25651 |
LitVar | rs25651 |
Map | rs25651 |
PheGenI | rs25651 |
Biobank | rs25651 |
1000 genomes | rs25651 |
hgdp | rs25651 |
ensembl | rs25651 |
geneview | rs25651 |
scholar | rs25651 |
rs25651 | |
pharmgkb | rs25651 |
gwascentral | rs25651 |
openSNP | rs25651 |
23andMe | rs25651 |
SNPshot | rs25651 |
SNPdbe | rs25651 |
MSV3d | rs25651 |
GWAS Ctlg | rs25651 |
GMAF | 0.3154 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18682748] Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction.
[PMID 21881118] Genetic variants and susceptibility to neurological complications following West Nile virus infection.