rs4144242
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4144242(A;A) |
Make rs4144242(A;G) |
Make rs4144242(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 40714789 |
Gene | RAD51 |
is a | snp |
is | mentioned by |
dbSNP | rs4144242 |
dbSNP (classic) | rs4144242 |
ClinGen | rs4144242 |
ebi | rs4144242 |
HLI | rs4144242 |
Exac | rs4144242 |
Gnomad | rs4144242 |
Varsome | rs4144242 |
LitVar | rs4144242 |
Map | rs4144242 |
PheGenI | rs4144242 |
Biobank | rs4144242 |
1000 genomes | rs4144242 |
hgdp | rs4144242 |
ensembl | rs4144242 |
geneview | rs4144242 |
scholar | rs4144242 |
rs4144242 | |
pharmgkb | rs4144242 |
gwascentral | rs4144242 |
openSNP | rs4144242 |
23andMe | rs4144242 |
SNPshot | rs4144242 |
SNPdbe | rs4144242 |
MSV3d | rs4144242 |
GWAS Ctlg | rs4144242 |
GMAF | 0.1446 |
Max Magnitude | 0 |
? | (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 17999359] RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.