rs17884306
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs17884306(A;A) |
Make rs17884306(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 7668783 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs17884306 |
dbSNP (classic) | rs17884306 |
ClinGen | rs17884306 |
ebi | rs17884306 |
HLI | rs17884306 |
Exac | rs17884306 |
Gnomad | rs17884306 |
Varsome | rs17884306 |
LitVar | rs17884306 |
Map | rs17884306 |
PheGenI | rs17884306 |
Biobank | rs17884306 |
1000 genomes | rs17884306 |
hgdp | rs17884306 |
ensembl | rs17884306 |
geneview | rs17884306 |
scholar | rs17884306 |
rs17884306 | |
pharmgkb | rs17884306 |
gwascentral | rs17884306 |
openSNP | rs17884306 |
23andMe | rs17884306 |
SNPshot | rs17884306 |
SNPdbe | rs17884306 |
MSV3d | rs17884306 |
GWAS Ctlg | rs17884306 |
GMAF | 0.05418 |
Max Magnitude | 0 |
[PMID 20110284] Genotype and haplotype analysis of TP53 gene and the risk of pancreatic cancer: an association study in the Czech Republic
[PMID 18640487] Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation.
[PMID 19224585] Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic.
[PMID 19500380] LD2SNPing: linkage disequilibrium plotter and RFLP enzyme mining for tag SNPs.
ClinVar | |
---|---|
Risk | rs17884306(A;A) |
Alt | rs17884306(A;A) |
Reference | Rs17884306(G;G) |
Significance | Probable-non-pathogenic |
Disease | Li-Fraumeni syndrome |
Variation | info |
Gene | TP53 |
CLNDBN | Li-Fraumeni syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.7572101C>T |
CLNSRC | |
CLNACC | RCV000401514.1, |