rs1878703
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1878703(C;C) |
Make rs1878703(C;G) |
Make rs1878703(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 14 |
Position | 20452590 |
Gene | OSGEP |
is a | snp |
is | mentioned by |
dbSNP | rs1878703 |
dbSNP (classic) | rs1878703 |
ClinGen | rs1878703 |
ebi | rs1878703 |
HLI | rs1878703 |
Exac | rs1878703 |
Gnomad | rs1878703 |
Varsome | rs1878703 |
LitVar | rs1878703 |
Map | rs1878703 |
PheGenI | rs1878703 |
Biobank | rs1878703 |
1000 genomes | rs1878703 |
hgdp | rs1878703 |
ensembl | rs1878703 |
geneview | rs1878703 |
scholar | rs1878703 |
rs1878703 | |
pharmgkb | rs1878703 |
gwascentral | rs1878703 |
openSNP | rs1878703 |
23andMe | rs1878703 |
SNPshot | rs1878703 |
SNPdbe | rs1878703 |
MSV3d | rs1878703 |
GWAS Ctlg | rs1878703 |
Max Magnitude | 0 |
[PMID 25703835] Genetic variants in the DNA repair gene NEIL3 and the risk of myocardial infarction in a nested case-control study. The HUNT Study