rs3748570
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3748570(A;A) |
Make rs3748570(A;G) |
Make rs3748570(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 156670364 |
Gene | NES |
is a | snp |
is | mentioned by |
dbSNP | rs3748570 |
dbSNP (classic) | rs3748570 |
ClinGen | rs3748570 |
ebi | rs3748570 |
HLI | rs3748570 |
Exac | rs3748570 |
Gnomad | rs3748570 |
Varsome | rs3748570 |
LitVar | rs3748570 |
Map | rs3748570 |
PheGenI | rs3748570 |
Biobank | rs3748570 |
1000 genomes | rs3748570 |
hgdp | rs3748570 |
ensembl | rs3748570 |
geneview | rs3748570 |
scholar | rs3748570 |
rs3748570 | |
pharmgkb | rs3748570 |
gwascentral | rs3748570 |
openSNP | rs3748570 |
23andMe | rs3748570 |
SNPshot | rs3748570 |
SNPdbe | rs3748570 |
MSV3d | rs3748570 |
GWAS Ctlg | rs3748570 |
GMAF | 0.2695 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18724036] Variants in the nestin gene and coronary heart disease