rs11067228
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11067228(A;A) |
Make rs11067228(A;G) |
Make rs11067228(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 114656455 |
is a | snp |
is | mentioned by |
dbSNP | rs11067228 |
dbSNP (classic) | rs11067228 |
ClinGen | rs11067228 |
ebi | rs11067228 |
HLI | rs11067228 |
Exac | rs11067228 |
Gnomad | rs11067228 |
Varsome | rs11067228 |
LitVar | rs11067228 |
Map | rs11067228 |
PheGenI | rs11067228 |
Biobank | rs11067228 |
1000 genomes | rs11067228 |
hgdp | rs11067228 |
ensembl | rs11067228 |
geneview | rs11067228 |
scholar | rs11067228 |
rs11067228 | |
pharmgkb | rs11067228 |
gwascentral | rs11067228 |
openSNP | rs11067228 |
23andMe | rs11067228 |
SNPshot | rs11067228 |
SNPdbe | rs11067228 |
MSV3d | rs11067228 |
GWAS Ctlg | rs11067228 |
GMAF | 0.3618 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21160077] |
Trait | |
Title | Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels |
Risk Allele | A |
P-val | 2E-11 |
Odds Ratio | 8.3000 [NR] % increase |
[PMID 23937305] Validation of association of genetic variants at 10q with prostate-specific antigen (PSA) levels in men at high risk for prostate cancer
[PMID 23246478] Personalized prostate specific antigen testing using genetic variants may reduce unnecessary prostate biopsies.