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rs17887200

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17887200(A;G)
Make rs17887200(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7667753
GeneTP53
is asnp
is mentioned by
dbSNPrs17887200
ebirs17887200
HLIrs17887200
Exacrs17887200
Varsomers17887200
Maprs17887200
PheGenIrs17887200
hapmaprs17887200
1000 genomesrs17887200
hgdprs17887200
ensemblrs17887200
gopubmedrs17887200
geneviewrs17887200
scholarrs17887200
googlers17887200
pharmgkbrs17887200
gwascentralrs17887200
openSNPrs17887200
23andMers17887200
23andMe allrs17887200
SNP Nexus

SNPshotrs17887200
SNPdbers17887200
MSV3drs17887200
GWAS Ctlgrs17887200
GMAF0.1511
Max Magnitude0
[PMID 17683073] rs17887200 and rs12951053 associated with ER negative breast cancer tumors (1.48 (1.11-1.93) p-trend = 0.01 and 1.29 (1.06-1.58) p-trend = 0.009, respectively)


[PMID 17428325OA-icon.png] Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.


[PMID 19423538OA-icon.png] Common genetic variation in TP53 and risk of human papillomavirus persistence and progression to CIN3/cancer revisited.