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rs17883323

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17883323(A;A)
Make rs17883323(A;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position7676301
GeneTP53
is asnp
is mentioned by
dbSNPrs17883323
dbSNP (old)rs17883323
ClinGenrs17883323
ebirs17883323
HLIrs17883323
Exacrs17883323
Varsomers17883323
Maprs17883323
PheGenIrs17883323
Biobankrs17883323
1000 genomesrs17883323
hgdprs17883323
ensemblrs17883323
gopubmedrs17883323
geneviewrs17883323
scholarrs17883323
googlers17883323
pharmgkbrs17883323
gwascentralrs17883323
openSNPrs17883323
23andMers17883323
23andMe allrs17883323
SNP Nexus

SNPshotrs17883323
SNPdbers17883323
MSV3drs17883323
GWAS Ctlgrs17883323
GMAF0.07346
Max Magnitude0

[PMID 24324286OA-icon.png] Investigation of genetic polymorphisms related to the outcome of radiotherapy for prostate cancer patients


[PMID 18849522OA-icon.png] Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes.


[PMID 19426493OA-icon.png] A case-control study on the combined effects of p53 and p73 polymorphisms on head and neck cancer risk in an Italian population.


ClinVar
Risk rs17883323(A;A)
Alt rs17883323(A;A)
Reference Rs17883323(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene TP53
CLNDBN not specified
Reversed 1
HGVS NC_000017.10:g.7579619G>T
CLNSRC
CLNACC RCV000242439.1,