rs2107425
| Orientation | plus |
| Stabilized | plus |
| Make rs2107425(C;C) |
| Make rs2107425(C;T) |
| Make rs2107425(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 1999845 |
| Gene | H19, MRPL23 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2107425 |
| dbSNP (classic) | rs2107425 |
| ClinGen | rs2107425 |
| ebi | rs2107425 |
| HLI | rs2107425 |
| Exac | rs2107425 |
| Gnomad | rs2107425 |
| Varsome | rs2107425 |
| LitVar | rs2107425 |
| Map | rs2107425 |
| PheGenI | rs2107425 |
| Biobank | rs2107425 |
| 1000 genomes | rs2107425 |
| hgdp | rs2107425 |
| ensembl | rs2107425 |
| geneview | rs2107425 |
| scholar | rs2107425 |
| rs2107425 | |
| pharmgkb | rs2107425 |
| gwascentral | rs2107425 |
| openSNP | rs2107425 |
| 23andMe | rs2107425 |
| SNPshot | rs2107425 |
| SNPdbe | rs2107425 |
| MSV3d | rs2107425 |
| GWAS Ctlg | rs2107425 |
| GMAF | 0.4164 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19543528
] 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 16839189] Human imprinted chromosomal regions are historical hot-spots of recombination.
[PMID 18224312] 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 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 19304784] Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study.
[PMID 19330030] A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).
[PMID 19639606] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
[PMID 19936258] Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1.
[PMID 20085711] Leveraging genetic variability across populations for the identification of causal variants.
[PMID 20159110] Allelic skewing of DNA methylation is widespread across the genome.
[PMID 22907587] IGF2 DNA methylation is a modulator of newborn's fetal growth and development.
