rs1799794
| Orientation | minus |
| Stabilized | minus |
| Make rs1799794(A;A) |
| Make rs1799794(A;G) |
| Make rs1799794(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 103712930 |
| Gene | LOC107984648, XRCC3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799794 |
| dbSNP (classic) | rs1799794 |
| ClinGen | rs1799794 |
| ebi | rs1799794 |
| HLI | rs1799794 |
| Exac | rs1799794 |
| Gnomad | rs1799794 |
| Varsome | rs1799794 |
| LitVar | rs1799794 |
| Map | rs1799794 |
| PheGenI | rs1799794 |
| Biobank | rs1799794 |
| 1000 genomes | rs1799794 |
| hgdp | rs1799794 |
| ensembl | rs1799794 |
| geneview | rs1799794 |
| scholar | rs1799794 |
| rs1799794 | |
| pharmgkb | rs1799794 |
| gwascentral | rs1799794 |
| openSNP | rs1799794 |
| 23andMe | rs1799794 |
| SNPshot | rs1799794 |
| SNPdbe | rs1799794 |
| MSV3d | rs1799794 |
| GWAS Ctlg | rs1799794 |
| GMAF | 0.2645 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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[PMID 21725594] Combined effect of polymorphisms in Rad51 and Xrcc3 on breast cancer risk and chromosomal radiosensitivity
[PMID 16465622
] Bladder cancer predisposition: a multigenic approach to DNA-repair and cell-cycle-control genes.
[PMID 18768505] Genetic susceptibility to renal cell carcinoma: the role of DNA double-strand break repair pathway.
[PMID 19276285] Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.
[PMID 20808897] Disease-associated mutations that alter the RNA structural ensemble.
[PMID 21347786] DNA repair gene and MTHFR gene polymorphisms as prognostic markers in locally advanced adenocarcinoma of the esophagus or stomach treated with cisplatin and 5-fluorouracil-based neoadjuvant chemotherapy.
[PMID 23075580] Association of a XRCC3 polymorphism and rectum mean dose with the risk of acute radio-induced gastrointestinal toxicity in prostate cancer patients
[PMID 22868256] A prospective validation pharmacogenomic study in the adjuvant setting of colorectal cancer patients treated with the 5-fluorouracil/leucovorin/oxaliplatin (FOLFOX4) regimen.
[PMID 23924833] Association of XRCC3 and XRCC4 gene polymorphisms, family history of cancer and tobacco smoking with non-small-cell lung cancer in a Chinese population: a case-control study
[PMID 24922659] Contribution of DNA Double-strand Break Repair Gene XRCC3 Genotypes to Oral Cancer Susceptibility in Taiwan
[PMID 25006581] Analyzing Association of the XRCC3 Gene Polymorphism with Ovarian Cancer Risk
[PMID 25176580] NBN and XRCC3 genetic variants in childhood acute lymphoblastic leukaemia
[PMID 26254358] Contribution of X-Ray Repair Complementing Defective Repair in Chinese Hamster Cells 3 (XRCC3) Genotype to Leiomyoma Risk
[PMID 26543082] Contribution of DNA Double-strand Break Repair Gene XRCC3 Genotypes to Triple-negative Breast Cancer Risk
[PMID 26938431] Association Studies Between XRCC1, XRCC2, XRCC3 Polymorphisms and Differentiated Thyroid Carcinoma.
