rs9832625
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9832625(A;A) |
Make rs9832625(A;C) |
Make rs9832625(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 3 |
Position | 29287529 |
Gene | RBMS3 |
is a | snp |
is | mentioned by |
dbSNP | rs9832625 |
dbSNP (classic) | rs9832625 |
ClinGen | rs9832625 |
ebi | rs9832625 |
HLI | rs9832625 |
Exac | rs9832625 |
Gnomad | rs9832625 |
Varsome | rs9832625 |
LitVar | rs9832625 |
Map | rs9832625 |
PheGenI | rs9832625 |
Biobank | rs9832625 |
1000 genomes | rs9832625 |
hgdp | rs9832625 |
ensembl | rs9832625 |
geneview | rs9832625 |
scholar | rs9832625 |
rs9832625 | |
pharmgkb | rs9832625 |
gwascentral | rs9832625 |
openSNP | rs9832625 |
23andMe | rs9832625 |
SNPshot | rs9832625 |
SNPdbe | rs9832625 |
MSV3d | rs9832625 |
GWAS Ctlg | rs9832625 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24785509] |
Trait | Response to radiotherapy in cancer (late toxicity) |
Title | A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicity. |
Risk Allele | |
P-val | 3E-6 |
Odds Ratio | .07 [NR] unit increase |