rs8064946
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8064946(C;C) |
Make rs8064946(C;G) |
Make rs8064946(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 7685993 |
Gene | TP53, WRAP53 |
is a | snp |
is | mentioned by |
dbSNP | rs8064946 |
dbSNP (classic) | rs8064946 |
ClinGen | rs8064946 |
ebi | rs8064946 |
HLI | rs8064946 |
Exac | rs8064946 |
Gnomad | rs8064946 |
Varsome | rs8064946 |
LitVar | rs8064946 |
Map | rs8064946 |
PheGenI | rs8064946 |
Biobank | rs8064946 |
1000 genomes | rs8064946 |
hgdp | rs8064946 |
ensembl | rs8064946 |
geneview | rs8064946 |
scholar | rs8064946 |
rs8064946 | |
pharmgkb | rs8064946 |
gwascentral | rs8064946 |
openSNP | rs8064946 |
23andMe | rs8064946 |
SNPshot | rs8064946 |
SNPdbe | rs8064946 |
MSV3d | rs8064946 |
GWAS Ctlg | rs8064946 |
GMAF | 0.3476 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 23836507] Association between TP53 R249S mutation and polymorphisms in TP53 intron 1 in hepatocellular carcinoma [PMID 15450681] Tumor suppressor gene TP53 is genetically associated with schizophrenia in the Chinese population.
[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 30686012] TP53 rs1042522 and rs8064946 variants in myocardial infarction.