rs12769288
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12769288(C;C) |
Make rs12769288(C;T) |
Make rs12769288(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 129488086 |
Gene | MGMT |
is a | snp |
is | mentioned by |
dbSNP | rs12769288 |
dbSNP (classic) | rs12769288 |
ClinGen | rs12769288 |
ebi | rs12769288 |
HLI | rs12769288 |
Exac | rs12769288 |
Gnomad | rs12769288 |
Varsome | rs12769288 |
LitVar | rs12769288 |
Map | rs12769288 |
PheGenI | rs12769288 |
Biobank | rs12769288 |
1000 genomes | rs12769288 |
hgdp | rs12769288 |
ensembl | rs12769288 |
geneview | rs12769288 |
scholar | rs12769288 |
rs12769288 | |
pharmgkb | rs12769288 |
gwascentral | rs12769288 |
openSNP | rs12769288 |
23andMe | rs12769288 |
SNPshot | rs12769288 |
SNPdbe | rs12769288 |
MSV3d | rs12769288 |
GWAS Ctlg | rs12769288 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 29263185] Germline variants in DNA repair genes, diagnostic radiation and risk of thyroid cancer.