rs4973768
Orientation | plus |
Stabilized | plus |
Make rs4973768(C;C) |
Make rs4973768(C;T) |
Make rs4973768(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 27374522 |
Gene | SLC4A7 |
is a | snp |
is | mentioned by |
dbSNP | rs4973768 |
dbSNP (classic) | rs4973768 |
ClinGen | rs4973768 |
ebi | rs4973768 |
HLI | rs4973768 |
Exac | rs4973768 |
Gnomad | rs4973768 |
Varsome | rs4973768 |
LitVar | rs4973768 |
Map | rs4973768 |
PheGenI | rs4973768 |
Biobank | rs4973768 |
1000 genomes | rs4973768 |
hgdp | rs4973768 |
ensembl | rs4973768 |
geneview | rs4973768 |
scholar | rs4973768 |
rs4973768 | |
pharmgkb | rs4973768 |
gwascentral | rs4973768 |
openSNP | rs4973768 |
23andMe | rs4973768 |
SNPshot | rs4973768 |
SNPdbe | rs4973768 |
MSV3d | rs4973768 |
GWAS Ctlg | rs4973768 |
GMAF | 0.3669 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20453838] |
Trait | Breast cancer |
Title | Genome-wide association study identifies five new breast cancer susceptibility loci |
Risk Allele | T |
P-val | 6E-7 |
Odds Ratio | 1.16 [1.10-1.24] |
[PMID 20699374] Evaluation of Breast Cancer Susceptibility Loci in Chinese Women
[PMID 21118973] Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction
GWAS snp | |
---|---|
PMID | [PMID 21263130] |
Trait | |
Title | Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study |
Risk Allele | C |
P-val | 2E-8 |
Odds Ratio | 1.1400 [1.09-1.19] |
[PMID 21415360] Common genetic variants associated with breast cancer in Korean women and differential susceptibility according to intrinsic subtype
[PMID 21445572] Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies
[PMID 21791674] Interactions Between Genetic Variants and Breast Cancer Risk Factors in the Breast and Prostate Cancer Cohort Consortium
[PMID 22287734] Evaluation of Breast Cancer Susceptibility Loci on 2q35, 3p24, 17q23 and FGFR2 Genes in Taiwanese Women with Breast Cancer
[PMID 19330027] Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
[PMID 19639606] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
[PMID 20146796] Familial relative risks for breast cancer by pathological subtype: a population-based cohort study.
[PMID 21596841] Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.
[PMID 22160591] A genetic risk predictor for breast cancer using a combination of low-penetrance polymorphisms in a Japanese population.
[PMID 22532573] The role of genetic breast cancer susceptibility variants as prognostic factors.
[PMID 23117855] The SLC4A7 variant rs4973768 is associated with breast cancer risk: evidence from a case-control study and a meta-analysis
GWAS snp | |
---|---|
PMID | [PMID 23535729] |
Trait | Breast cancer |
Title | Large-scale genotyping identifies 41 new loci associated with breast cancer risk. |
Risk Allele | T |
P-val | 2E-30 |
Odds Ratio | 1.10 [1.08-1.12] |
[PMID 25784121] Associations between breast density and a panel of single nucleotide polymorphisms linked to breast cancer risk: a cohort study with digital mammography
[PMID 25881232] Associations between breast density and a panel of single nucleotide polymorphisms linked to breast cancer risk: a cohort study with digital mammography
[PMID 24895409] Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women
[PMID 27609814] Oncogenic p95HER2 regulates Na+-HCO3- cotransporter NBCn1 mRNA stability in breast cancer cells via 3'UTR dependent processes.
[PMID 27863437] Association of multiple genetic variants with breast cancer susceptibility in the Han Chinese population.
[PMID 28757652] Genetic Breast Cancer Susceptibility Variants and Prognosis in the Prospectively Randomized SUCCESS A Study.
[PMID 32366738] Low-penetrance susceptibility variants and postmenopausal oestrogen receptor positive breast cancer.