rs13390641
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13390641(A;A) |
Make rs13390641(A;G) |
Make rs13390641(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 103419975 |
is a | snp |
is | mentioned by |
dbSNP | rs13390641 |
dbSNP (classic) | rs13390641 |
ClinGen | rs13390641 |
ebi | rs13390641 |
HLI | rs13390641 |
Exac | rs13390641 |
Gnomad | rs13390641 |
Varsome | rs13390641 |
LitVar | rs13390641 |
Map | rs13390641 |
PheGenI | rs13390641 |
Biobank | rs13390641 |
1000 genomes | rs13390641 |
hgdp | rs13390641 |
ensembl | rs13390641 |
geneview | rs13390641 |
scholar | rs13390641 |
rs13390641 | |
pharmgkb | rs13390641 |
gwascentral | rs13390641 |
openSNP | rs13390641 |
23andMe | rs13390641 |
SNPshot | rs13390641 |
SNPdbe | rs13390641 |
MSV3d | rs13390641 |
GWAS Ctlg | rs13390641 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24903457] Identification of a genetic variant at 2q12.1 associated with blood pressure in East-Asians by genome-wide scan including gene-environment interactions