Have questions? Visit https://www.reddit.com/r/SNPedia

rs35117667

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35117667(C;T)
Make rs35117667(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position7676278
GeneTP53
is asnp
is mentioned by
dbSNPrs35117667
ebirs35117667
HLIrs35117667
Exacrs35117667
Varsomers35117667
Maprs35117667
PheGenIrs35117667
hapmaprs35117667
1000 genomesrs35117667
hgdprs35117667
ensemblrs35117667
gopubmedrs35117667
geneviewrs35117667
scholarrs35117667
googlers35117667
pharmgkbrs35117667
gwascentralrs35117667
openSNPrs35117667
23andMers35117667
23andMe allrs35117667
SNP Nexus

SNPshotrs35117667
SNPdbers35117667
MSV3drs35117667
GWAS Ctlgrs35117667
GMAF0.00551
Max Magnitude0

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

ClinVar
Risk rs35117667(T;T)
Alt rs35117667(T;T)
Reference rs35117667(C;C)
Significance Non-pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7579596G>A
CLNSRC
CLNACC RCV000206386.2,