rs6489769
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6489769(C;C) |
Make rs6489769(C;T) |
Make rs6489769(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 963799 |
Gene | RAD52 |
is a | snp |
is | mentioned by |
dbSNP | rs6489769 |
dbSNP (classic) | rs6489769 |
ClinGen | rs6489769 |
ebi | rs6489769 |
HLI | rs6489769 |
Exac | rs6489769 |
Gnomad | rs6489769 |
Varsome | rs6489769 |
LitVar | rs6489769 |
Map | rs6489769 |
PheGenI | rs6489769 |
Biobank | rs6489769 |
1000 genomes | rs6489769 |
hgdp | rs6489769 |
ensembl | rs6489769 |
geneview | rs6489769 |
scholar | rs6489769 |
rs6489769 | |
pharmgkb | rs6489769 |
gwascentral | rs6489769 |
openSNP | rs6489769 |
23andMe | rs6489769 |
SNPshot | rs6489769 |
SNPdbe | rs6489769 |
MSV3d | rs6489769 |
GWAS Ctlg | rs6489769 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25012956] A RAD52 genetic variant located in a miRNA binding site is associated with glioma risk in Han Chinese
[PMID 26629180] Identification of an SCLC susceptibility rs7963551 genetic polymorphism in a previously GWAS-identified 12p13.33 RAD52 lung cancer risk locus in the Chinese population.