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rs1800371

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs1800371(C;C)
Make rs1800371(C;T)
Make rs1800371(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position7676230
GeneTP53
is asnp
is mentioned by
dbSNPrs1800371
ebirs1800371
HLIrs1800371
Exacrs1800371
Varsomers1800371
Maprs1800371
PheGenIrs1800371
hapmaprs1800371
1000 genomesrs1800371
hgdprs1800371
ensemblrs1800371
gopubmedrs1800371
geneviewrs1800371
scholarrs1800371
googlers1800371
pharmgkbrs1800371
gwascentralrs1800371
openSNPrs1800371
23andMers1800371
23andMe allrs1800371
SNP Nexus

SNPshotrs1800371
SNPdbers1800371
MSV3drs1800371
GWAS Ctlgrs1800371
GMAF0.006428
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 24324286OA-icon.png] Investigation of genetic polymorphisms related to the outcome of radiotherapy for prostate cancer patients


[PMID 18212354OA-icon.png] Genes in glucose metabolism and association with spina bifida.


[PMID 18798306OA-icon.png] Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.


[PMID 19784392OA-icon.png] Primary open angle glaucoma in a Caucasian population is associated with the p53 codon 72 polymorphism.


ClinVar
Risk rs1800371(T;T)
Alt rs1800371(T;T)
Reference rs1800371(C;C)
Significance Other
Disease not specified Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1 Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN not specified Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1 Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7579548G>A
CLNSRC Ambry Genetics ClinVar GeneDx
CLNACC RCV000036530.4, RCV000131567.4, RCV000172826.1, RCV000203736.2,



[PMID 25935255] TP53 polymorphism may contribute to genetic susceptibility to develop Hashimoto's thyroiditis