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rs2107425

From SNPedia

Orientationplus
Stabilizedplus
Make rs2107425(C;C)
Make rs2107425(C;T)
Make rs2107425(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position1999845
is asnp
is mentioned by
dbSNPrs2107425
ebirs2107425
HLIrs2107425
Exacrs2107425
Varsomers2107425
Maprs2107425
PheGenIrs2107425
hapmaprs2107425
1000 genomesrs2107425
hgdprs2107425
ensemblrs2107425
gopubmedrs2107425
geneviewrs2107425
scholarrs2107425
googlers2107425
pharmgkbrs2107425
gwascentralrs2107425
openSNPrs2107425
23andMers2107425
23andMe allrs2107425
SNP Nexus

SNPshotrs2107425
SNPdbers2107425
MSV3drs2107425
GWAS Ctlgrs2107425
GMAF0.4164
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19543528OA-icon.png] Association between Common Germline Genetic Variation in 94 Candidate Genes or Regions and Risks of Invasive Epithelial Ovarian Cancer


[PMID 20145138] Common genetic variants associated with breast cancer and mammographic density measures that predict disease


[PMID 21748294] Correlation of breast cancer susceptibility loci with patient characteristics, metastasis-free survival, and mRNA expression of the nearest genes


[PMID 16839189OA-icon.png] Human imprinted chromosomal regions are historical hot-spots of recombination.


[PMID 18224312OA-icon.png] Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment.


[PMID 18262338] Polymorphisms in the H19 gene and the risk of bladder cancer.


[PMID 18681954OA-icon.png] Breast cancer susceptibility loci and mammographic density.


[PMID 18708391OA-icon.png] Breast cancer risk polymorphisms and interaction with ionizing radiation among U.S. radiologic technologists.


[PMID 19304784OA-icon.png] Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study.


[PMID 19330030OA-icon.png] A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).


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


[PMID 19936258OA-icon.png] Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1.


[PMID 20085711OA-icon.png] Leveraging genetic variability across populations for the identification of causal variants.


[PMID 20159110OA-icon.png] Allelic skewing of DNA methylation is widespread across the genome.


[PMID 22907587OA-icon.png] IGF2 DNA methylation is a modulator of newborn's fetal growth and development.