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rs36228499

From SNPedia

Orientationminus
Stabilizedminus
Make rs36228499(G;G)
Make rs36228499(G;T)
Make rs36228499(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position12717002
GeneCDKN1B, LOC101929220
is asnp
is mentioned by
dbSNPrs36228499
ebirs36228499
HLIrs36228499
Exacrs36228499
Varsomers36228499
Maprs36228499
PheGenIrs36228499
hapmaprs36228499
1000 genomesrs36228499
hgdprs36228499
ensemblrs36228499
gopubmedrs36228499
geneviewrs36228499
scholarrs36228499
googlers36228499
pharmgkbrs36228499
gwascentralrs36228499
openSNPrs36228499
23andMers36228499
23andMe allrs36228499
SNP Nexus

SNPshotrs36228499
SNPdbers36228499
MSV3drs36228499
GWAS Ctlgrs36228499
GMAF0.3976
Max Magnitude

[PMID 20075119] Allelic variant at -79 (C>T) in CDKNIB (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels [PMID 19667240] p27kip1-838C>A single nucleotide polymorphism is associated with restenosis risk after coronary stenting and modulates p27kip1 promoter activity.


[PMID 20617153OA-icon.png] Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemia.

[PMID 23966119OA-icon.png] Genetic Risk Factors for Hypertrophic Scar Development