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

rs4144242

From SNPedia

Orientationplus
Stabilizedplus
Make rs4144242(A;A)
Make rs4144242(A;G)
Make rs4144242(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position40714789
GeneRAD51
is asnp
is mentioned by
dbSNPrs4144242
ebirs4144242
HLIrs4144242
Exacrs4144242
Varsomers4144242
Maprs4144242
PheGenIrs4144242
hapmaprs4144242
1000 genomesrs4144242
hgdprs4144242
ensemblrs4144242
gopubmedrs4144242
geneviewrs4144242
scholarrs4144242
googlers4144242
pharmgkbrs4144242
gwascentralrs4144242
openSNPrs4144242
23andMers4144242
23andMe allrs4144242
SNP Nexus

SNPshotrs4144242
SNPdbers4144242
MSV3drs4144242
GWAS Ctlgrs4144242
GMAF0.1446
Max Magnitude
? (A;A) (A;G) (G;G) 28

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


[PMID 17999359OA-icon.png] RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.