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rs17884306

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17884306(A;A)
Make rs17884306(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7668783
GeneTP53
is asnp
is mentioned by
dbSNPrs17884306
dbSNP (classic)rs17884306
ClinGenrs17884306
ebirs17884306
HLIrs17884306
Exacrs17884306
Gnomadrs17884306
Varsomers17884306
LitVarrs17884306
Maprs17884306
PheGenIrs17884306
Biobankrs17884306
1000 genomesrs17884306
hgdprs17884306
ensemblrs17884306
geneviewrs17884306
scholarrs17884306
googlers17884306
pharmgkbrs17884306
gwascentralrs17884306
openSNPrs17884306
23andMers17884306
SNPshotrs17884306
SNPdbers17884306
MSV3drs17884306
GWAS Ctlgrs17884306
GMAF0.05418
Max Magnitude0

[PMID 20110284] Genotype and haplotype analysis of TP53 gene and the risk of pancreatic cancer: an association study in the Czech Republic


[PMID 18640487OA-icon.png] Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation.


[PMID 19224585] Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic.


[PMID 19500380OA-icon.png] LD2SNPing: linkage disequilibrium plotter and RFLP enzyme mining for tag SNPs.


ClinVar
Risk rs17884306(A;A)
Alt rs17884306(A;A)
Reference Rs17884306(G;G)
Significance Probable-non-pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7572101C>T
CLNSRC
CLNACC RCV000401514.1,