Have questions? Visit https://www.reddit.com/r/SNPedia

rs4973768

From SNPedia

Orientationplus
Stabilizedplus
Make rs4973768(C;C)
Make rs4973768(C;T)
Make rs4973768(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position27374522
GeneSLC4A7
is asnp
is mentioned by
dbSNPrs4973768
ebirs4973768
HLIrs4973768
Exacrs4973768
Varsomers4973768
Maprs4973768
PheGenIrs4973768
hapmaprs4973768
1000 genomesrs4973768
hgdprs4973768
ensemblrs4973768
gopubmedrs4973768
geneviewrs4973768
scholarrs4973768
googlers4973768
pharmgkbrs4973768
gwascentralrs4973768
openSNPrs4973768
23andMers4973768
23andMe allrs4973768
SNP Nexus

SNPshotrs4973768
SNPdbers4973768
MSV3drs4973768
GWAS Ctlgrs4973768
GMAF0.3669
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20453838OA-icon.png]
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 20699374OA-icon.png] Evaluation of Breast Cancer Susceptibility Loci in Chinese Women

[PMID 21118973OA-icon.png] Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

OMIM114480
Desc
Variant
Relatedalso
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 21791674OA-icon.png] 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 19330027OA-icon.png] Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.


[PMID 19639606OA-icon.png] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.


[PMID 20146796OA-icon.png] Familial relative risks for breast cancer by pathological subtype: a population-based cohort study.


[PMID 21596841OA-icon.png] 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 22532573OA-icon.png] 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 23535729OA-icon.png]
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 25881232OA-icon.png] Associations between breast density and a panel of single nucleotide polymorphisms linked to breast cancer risk: a cohort study with digital mammography


[PMID 24895409OA-icon.png] 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.