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rs1049606

From SNPedia

Orientationplus
Stabilizedplus
Make rs1049606(C;C)
Make rs1049606(C;T)
Make rs1049606(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position4273870
GeneCCND2
is asnp
is mentioned by
dbSNPrs1049606
ebirs1049606
HLIrs1049606
Exacrs1049606
Varsomers1049606
Maprs1049606
PheGenIrs1049606
hapmaprs1049606
1000 genomesrs1049606
hgdprs1049606
ensemblrs1049606
gopubmedrs1049606
geneviewrs1049606
scholarrs1049606
googlers1049606
pharmgkbrs1049606
gwascentralrs1049606
openSNPrs1049606
23andMers1049606
23andMe allrs1049606
SNP Nexus

SNPshotrs1049606
SNPdbers1049606
MSV3drs1049606
GWAS Ctlgrs1049606
GMAF0.3838
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20414251] CCND2 polymorphisms associated with clearance of HBV Infection

[PMID 17267408OA-icon.png] Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.

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

[PMID 22004425] Genetic risk of hepatocellular carcinoma in patients with hepatitis C virus: a case control study.