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rs1800370

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1800370(A;A)
Make rs1800370(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position7676261
GeneTP53
is asnp
is mentioned by
dbSNPrs1800370
ebirs1800370
HLIrs1800370
Exacrs1800370
Varsomers1800370
Maprs1800370
PheGenIrs1800370
hapmaprs1800370
1000 genomesrs1800370
hgdprs1800370
ensemblrs1800370
gopubmedrs1800370
geneviewrs1800370
scholarrs1800370
googlers1800370
pharmgkbrs1800370
gwascentralrs1800370
openSNPrs1800370
23andMers1800370
23andMe allrs1800370
SNP Nexus

SNPshotrs1800370
SNPdbers1800370
MSV3drs1800370
GWAS Ctlgrs1800370
GMAF0.0124
Max Magnitude0

[PMID 22545084OA-icon.png] Analysis of Tp53 Codon 72 Polymorphisms, Tp53 Mutations, and HPV Infection in Cutaneous Squamous Cell Carcinomas


[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 21115003] TP53 polymorphisms in gliomas from Indian patients: Study of codon 72 genotype, rs1642785, rs1800370 and 16 base pair insertion in intron-3.


ClinVar
Risk rs1800370(A;A)
Alt rs1800370(A;A)
Reference rs1800370(G;G)
Significance Non-pathogenic
Disease Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579579C>T
CLNSRC ClinVar Invitae
CLNACC RCV000119149.2, RCV000162410.1,



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