rs12652447
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12652447(A;A) |
Make rs12652447(A;G) |
Make rs12652447(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 15674526 |
Gene | FBXL7 |
is a | snp |
is | mentioned by |
dbSNP | rs12652447 |
dbSNP (classic) | rs12652447 |
ClinGen | rs12652447 |
ebi | rs12652447 |
HLI | rs12652447 |
Exac | rs12652447 |
Gnomad | rs12652447 |
Varsome | rs12652447 |
LitVar | rs12652447 |
Map | rs12652447 |
PheGenI | rs12652447 |
Biobank | rs12652447 |
1000 genomes | rs12652447 |
hgdp | rs12652447 |
ensembl | rs12652447 |
geneview | rs12652447 |
scholar | rs12652447 |
rs12652447 | |
pharmgkb | rs12652447 |
gwascentral | rs12652447 |
openSNP | rs12652447 |
23andMe | rs12652447 |
SNPshot | rs12652447 |
SNPdbe | rs12652447 |
MSV3d | rs12652447 |
GWAS Ctlg | rs12652447 |
GMAF | 0.4761 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 24528085] Breast Cancer Association Studies in a Han Chinese Population using 10 European-ancestry-associated Breast Cancer Susceptibility SNPs
[PMID 20418484] Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.