rs8051542
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
Make rs8051542(C;T) |
Make rs8051542(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 52500255 |
Gene | TOX3 |
is a | snp |
is | mentioned by |
dbSNP | rs8051542 |
dbSNP (classic) | rs8051542 |
ClinGen | rs8051542 |
ebi | rs8051542 |
HLI | rs8051542 |
Exac | rs8051542 |
Gnomad | rs8051542 |
Varsome | rs8051542 |
LitVar | rs8051542 |
Map | rs8051542 |
PheGenI | rs8051542 |
Biobank | rs8051542 |
1000 genomes | rs8051542 |
hgdp | rs8051542 |
ensembl | rs8051542 |
geneview | rs8051542 |
scholar | rs8051542 |
rs8051542 | |
pharmgkb | rs8051542 |
gwascentral | rs8051542 |
openSNP | rs8051542 |
23andMe | rs8051542 |
SNPshot | rs8051542 |
SNPdbe | rs8051542 |
MSV3d | rs8051542 |
GWAS Ctlg | rs8051542 |
GMAF | 0.3444 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20054709] Birth weight, breast cancer susceptibility loci, and breast cancer risk
[PMID 20699374] Evaluation of Breast Cancer Susceptibility Loci in Chinese Women
[PMID 20703937] Association between polymorphisms of trinucleotide repeat containing 9 gene and breast cancer risk: evidence from 62,005 subjects
[PMID 17997823] Clinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases.
[PMID 18681954] Breast cancer susceptibility loci and mammographic density.
[PMID 18708391] Breast cancer risk polymorphisms and interaction with ionizing radiation among U.S. radiologic technologists.
[PMID 19219042] Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.
[PMID 19639606] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
[PMID 20085711] Leveraging genetic variability across populations for the identification of causal variants.
[PMID 20213080] Genetic variants in trinucleotide repeat-containing 9 (TNRC9) are associated with risk of estrogen receptor positive breast cancer in a Chinese population.
[PMID 20484103] Genetic and clinical predictors for breast cancer risk assessment and stratification among Chinese women.
[PMID 20585626] Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium.
[PMID 22910930] Genome-Wide Association Studies (GWAS) breast cancer susceptibility loci in Arabs: susceptibility and prognostic implications in Tunisians.
[PMID 22983835] The association between polymorphisms in the leptin receptor gene and risk of breast cancer: a systematic review and pooled analysis.
[PMID 27572905] Genetic variants in FGFR2 and TNRC9 genes are associated with breast cancer risk in Pakistani women.