rs3212879
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3212879(-;-) |
Make rs3212879(-;G) |
Make rs3212879(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 69648711 |
Gene | CCND1 |
is a | snp |
is | mentioned by |
dbSNP | rs3212879 |
dbSNP (classic) | rs3212879 |
ClinGen | rs3212879 |
ebi | rs3212879 |
HLI | rs3212879 |
Exac | rs3212879 |
Gnomad | rs3212879 |
Varsome | rs3212879 |
LitVar | rs3212879 |
Map | rs3212879 |
PheGenI | rs3212879 |
Biobank | rs3212879 |
1000 genomes | rs3212879 |
hgdp | rs3212879 |
ensembl | rs3212879 |
geneview | rs3212879 |
scholar | rs3212879 |
rs3212879 | |
pharmgkb | rs3212879 |
gwascentral | rs3212879 |
openSNP | rs3212879 |
23andMe | rs3212879 |
SNPshot | rs3212879 |
SNPdbe | rs3212879 |
MSV3d | rs3212879 |
GWAS Ctlg | rs3212879 |
GMAF | 0.4881 |
Max Magnitude | 0 |
[PMID 19258477] Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.
[PMID 18174243] Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population.
[PMID 19124506] Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer.
[PMID 19543528] Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer.