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rs3212891

From SNPedia

Orientationplus
Stabilizedplus
Make rs3212891(A;A)
Make rs3212891(A;C)
Make rs3212891(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position69650739
GeneCCND1
is asnp
is mentioned by
dbSNPrs3212891
dbSNP (classic)rs3212891
ClinGenrs3212891
ebirs3212891
HLIrs3212891
Exacrs3212891
Gnomadrs3212891
Varsomers3212891
LitVarrs3212891
Maprs3212891
PheGenIrs3212891
Biobankrs3212891
1000 genomesrs3212891
hgdprs3212891
ensemblrs3212891
geneviewrs3212891
scholarrs3212891
googlers3212891
pharmgkbrs3212891
gwascentralrs3212891
openSNPrs3212891
23andMers3212891
SNPshotrs3212891
SNPdbers3212891
MSV3drs3212891
GWAS Ctlgrs3212891
GMAF0.3792
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 19258477OA-icon.png] Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.


[PMID 18174243OA-icon.png] Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population.


[PMID 19124506OA-icon.png] Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer.


[PMID 19543528OA-icon.png] Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer.