rs4662834
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4662834(A;A) |
Make rs4662834(A;G) |
Make rs4662834(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 128721268 |
is a | snp |
is | mentioned by |
dbSNP | rs4662834 |
dbSNP (classic) | rs4662834 |
ClinGen | rs4662834 |
ebi | rs4662834 |
HLI | rs4662834 |
Exac | rs4662834 |
Gnomad | rs4662834 |
Varsome | rs4662834 |
LitVar | rs4662834 |
Map | rs4662834 |
PheGenI | rs4662834 |
Biobank | rs4662834 |
1000 genomes | rs4662834 |
hgdp | rs4662834 |
ensembl | rs4662834 |
geneview | rs4662834 |
scholar | rs4662834 |
rs4662834 | |
pharmgkb | rs4662834 |
gwascentral | rs4662834 |
openSNP | rs4662834 |
23andMe | rs4662834 |
SNPshot | rs4662834 |
SNPdbe | rs4662834 |
MSV3d | rs4662834 |
GWAS Ctlg | rs4662834 |
GMAF | 0.3985 |
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 | 0.000005 |
Odds Ratio | 0.0800 [0.04-0.11] fewer chromatid breaks |