rs1800370
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs1800370(A;A) |
| Make rs1800370(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 17 |
| Position | 7676261 |
| Gene | TP53 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1800370 |
| dbSNP (classic) | rs1800370 |
| ClinGen | rs1800370 |
| ebi | rs1800370 |
| HLI | rs1800370 |
| Exac | rs1800370 |
| Gnomad | rs1800370 |
| Varsome | rs1800370 |
| LitVar | rs1800370 |
| Map | rs1800370 |
| PheGenI | rs1800370 |
| Biobank | rs1800370 |
| 1000 genomes | rs1800370 |
| hgdp | rs1800370 |
| ensembl | rs1800370 |
| geneview | rs1800370 |
| scholar | rs1800370 |
| rs1800370 | |
| pharmgkb | rs1800370 |
| gwascentral | rs1800370 |
| openSNP | rs1800370 |
| 23andMe | rs1800370 |
| SNPshot | rs1800370 |
| SNPdbe | rs1800370 |
| MSV3d | rs1800370 |
| GWAS Ctlg | rs1800370 |
| GMAF | 0.0124 |
| Max Magnitude | 0 |
[PMID 22545084
] Analysis of Tp53 Codon 72 Polymorphisms, Tp53 Mutations, and HPV Infection in Cutaneous Squamous Cell Carcinomas
[PMID 18798306] 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 | Other |
| Disease | Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome not specified |
| Variation | info |
| Gene | TP53 |
| CLNDBN | Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome not specified |
| Reversed | 1 |
| HGVS | NC_000017.10:g.7579579C>T |
| CLNSRC | ClinVar Invitae |
| CLNACC | RCV000119149.4, RCV000162410.1, RCV000244898.1, |
[PMID 25935255] TP53 polymorphism may contribute to genetic susceptibility to develop Hashimoto's thyroiditis
