rs55832599
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 7 | Li-Fraumeni Syndrome (predicted) |
(G;G) | 0 | common in clinvar |
Make rs55832599(A;A) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 7673821 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs55832599 |
dbSNP (classic) | rs55832599 |
ClinGen | rs55832599 |
ebi | rs55832599 |
HLI | rs55832599 |
Exac | rs55832599 |
Gnomad | rs55832599 |
Varsome | rs55832599 |
LitVar | rs55832599 |
Map | rs55832599 |
PheGenI | rs55832599 |
Biobank | rs55832599 |
1000 genomes | rs55832599 |
hgdp | rs55832599 |
ensembl | rs55832599 |
geneview | rs55832599 |
scholar | rs55832599 |
rs55832599 | |
pharmgkb | rs55832599 |
gwascentral | rs55832599 |
openSNP | rs55832599 |
23andMe | rs55832599 |
SNPshot | rs55832599 |
SNPdbe | rs55832599 |
MSV3d | rs55832599 |
GWAS Ctlg | rs55832599 |
Max Magnitude | 7 |
ClinVar | |
---|---|
Risk | rs55832599(A;A) |
Alt | rs55832599(A;A) |
Reference | Rs55832599(G;G) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | TP53 |
CLNDBN | Hereditary cancer-predisposing syndrome not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.7577139G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000130398.4, RCV000413074.1, |