rs708547
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs708547(A;A) |
Make rs708547(A;G) |
Make rs708547(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 56955143 |
is a | snp |
is | mentioned by |
dbSNP | rs708547 |
dbSNP (classic) | rs708547 |
ClinGen | rs708547 |
ebi | rs708547 |
HLI | rs708547 |
Exac | rs708547 |
Gnomad | rs708547 |
Varsome | rs708547 |
LitVar | rs708547 |
Map | rs708547 |
PheGenI | rs708547 |
Biobank | rs708547 |
1000 genomes | rs708547 |
hgdp | rs708547 |
ensembl | rs708547 |
geneview | rs708547 |
scholar | rs708547 |
rs708547 | |
pharmgkb | rs708547 |
gwascentral | rs708547 |
openSNP | rs708547 |
23andMe | rs708547 |
SNPshot | rs708547 |
SNPdbe | rs708547 |
MSV3d | rs708547 |
GWAS Ctlg | rs708547 |
GMAF | 0.1492 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21106707] |
Trait | |
Title | A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity |
Risk Allele | A |
P-val | 9E-7 |
Odds Ratio | 0.1800 [0.11-0.24] fewer chromatid breaks |