rs2296675
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2296675(A;A) |
Make rs2296675(A;G) |
Make rs2296675(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 129766734 |
Gene | MGMT |
is a | snp |
is | mentioned by |
dbSNP | rs2296675 |
dbSNP (classic) | rs2296675 |
ClinGen | rs2296675 |
ebi | rs2296675 |
HLI | rs2296675 |
Exac | rs2296675 |
Gnomad | rs2296675 |
Varsome | rs2296675 |
LitVar | rs2296675 |
Map | rs2296675 |
PheGenI | rs2296675 |
Biobank | rs2296675 |
1000 genomes | rs2296675 |
hgdp | rs2296675 |
ensembl | rs2296675 |
geneview | rs2296675 |
scholar | rs2296675 |
rs2296675 | |
pharmgkb | rs2296675 |
gwascentral | rs2296675 |
openSNP | rs2296675 |
23andMe | rs2296675 |
SNPshot | rs2296675 |
SNPdbe | rs2296675 |
MSV3d | rs2296675 |
GWAS Ctlg | rs2296675 |
GMAF | 0.1327 |
Max Magnitude | 0 |
[PMID 23027618] DNA repair gene variants in relation to overall cancer risk: A population-based study
[PMID 28499365] Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.