rs13088089
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13088089(A;A) |
Make rs13088089(A;C) |
Make rs13088089(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 117061175 |
is a | snp |
is | mentioned by |
dbSNP | rs13088089 |
dbSNP (classic) | rs13088089 |
ClinGen | rs13088089 |
ebi | rs13088089 |
HLI | rs13088089 |
Exac | rs13088089 |
Gnomad | rs13088089 |
Varsome | rs13088089 |
LitVar | rs13088089 |
Map | rs13088089 |
PheGenI | rs13088089 |
Biobank | rs13088089 |
1000 genomes | rs13088089 |
hgdp | rs13088089 |
ensembl | rs13088089 |
geneview | rs13088089 |
scholar | rs13088089 |
rs13088089 | |
pharmgkb | rs13088089 |
gwascentral | rs13088089 |
openSNP | rs13088089 |
23andMe | rs13088089 |
SNPshot | rs13088089 |
SNPdbe | rs13088089 |
MSV3d | rs13088089 |
GWAS Ctlg | rs13088089 |
GMAF | 0.1804 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
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[PMID 23920401] Genetic variants in nuclear factor-kappa B binding sites are associated with clinical outcomes in prostate cancer patients