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rs1801320

From SNPedia

Orientationplus
Stabilizedplus
Make rs1801320(C;C)
Make rs1801320(C;G)
Make rs1801320(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position40695330
GeneDLX3, RAD51
is asnp
is mentioned by
dbSNPrs1801320
ebirs1801320
HLIrs1801320
Exacrs1801320
Varsomers1801320
Maprs1801320
PheGenIrs1801320
hapmaprs1801320
1000 genomesrs1801320
hgdprs1801320
ensemblrs1801320
gopubmedrs1801320
geneviewrs1801320
scholarrs1801320
googlers1801320
pharmgkbrs1801320
gwascentralrs1801320
openSNPrs1801320
23andMers1801320
23andMe allrs1801320
SNP Nexus

SNPshotrs1801320
SNPdbers1801320
MSV3drs1801320
GWAS Ctlgrs1801320
GMAF0.1304
Max Magnitude
? (C;C) (C;G) (G;G) 28
rs1801320, also known as 135G>C, is a SNP in the 5'-untranslated region (UTR) of the RAD51 gene.

A meta-analysis of 12 studies involving 7,065 cases and 6,981 controls found no evidence for a significant association between rs1801320 and risk for breast cancer in non-BRCA1/BRCA1 carriers, contrary to a previous report.[PMID 20461453]

[PMID 17999359OA-icon.png] rs1801320 in the CIMBA study so perhaps breast cancer related


[PMID 21725594] Combined effect of polymorphisms in Rad51 and Xrcc3 on breast cancer risk and chromosomal radiosensitivity


[PMID 17889711] RAD51 135G>C polymorphism and risk of familial breast cancer in a South American population.


[PMID 19276285OA-icon.png] Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.


[PMID 19536092OA-icon.png] Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.


[PMID 19584272OA-icon.png] Modification of ovarian cancer risk by BRCA1/2-interacting genes in a multicenter cohort of BRCA1/2 mutation carriers.


[PMID 20386703OA-icon.png] Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer.


[PMID 21104022OA-icon.png] Polymorphisms in RAD51, XRCC2 and XRCC3 genes of the homologous recombination repair in colorectal cancer--a case control study.


[PMID 24568492] Equivocal Association of RAD51 Polymorphisms with Risk of Esophageal Squamous Cell Carcinoma in a Chinese Population


[PMID 24930116OA-icon.png] Association of polymorphisms in the 5' untranslated region of RAD51 gene with risk of endometrial cancer in the Polish population


[PMID 26339569OA-icon.png] Polymorphisms of Homologous Recombination RAD51, RAD51B, XRCC2, and XRCC3 Genes and the Risk of Prostate Cancer


[PMID 26974709] Polymorphisms in double strand break repair related genes influence radiosensitivity phenotype in lymphocytes from healthy individuals.