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rs3217869

From SNPedia

Orientationplus
Stabilizedplus
Make rs3217869(A;A)
Make rs3217869(A;G)
Make rs3217869(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position4290804
GeneCCND2
is asnp
is mentioned by
dbSNPrs3217869
ebirs3217869
HLIrs3217869
Exacrs3217869
Varsomers3217869
Maprs3217869
PheGenIrs3217869
hapmaprs3217869
1000 genomesrs3217869
hgdprs3217869
ensemblrs3217869
gopubmedrs3217869
geneviewrs3217869
scholarrs3217869
googlers3217869
pharmgkbrs3217869
gwascentralrs3217869
openSNPrs3217869
23andMers3217869
23andMe allrs3217869
SNP Nexus

SNPshotrs3217869
SNPdbers3217869
MSV3drs3217869
GWAS Ctlgrs3217869
GMAF0.3907
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23459443OA-icon.png]
Trait QT interval (interaction)
Title Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.
Risk Allele A
P-val 4E-6
Odds Ratio NR NR


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


[PMID 18281541OA-icon.png] Effects of common germ-line genetic variation in cell cycle genes on ovarian cancer survival.


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