rs587780068
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587780068(C;T) |
Make rs587780068(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 7675140 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs587780068 |
dbSNP (classic) | rs587780068 |
ClinGen | rs587780068 |
ebi | rs587780068 |
HLI | rs587780068 |
Exac | rs587780068 |
Gnomad | rs587780068 |
Varsome | rs587780068 |
LitVar | rs587780068 |
Map | rs587780068 |
PheGenI | rs587780068 |
Biobank | rs587780068 |
1000 genomes | rs587780068 |
hgdp | rs587780068 |
ensembl | rs587780068 |
geneview | rs587780068 |
scholar | rs587780068 |
rs587780068 | |
pharmgkb | rs587780068 |
gwascentral | rs587780068 |
openSNP | rs587780068 |
23andMe | rs587780068 |
SNPshot | rs587780068 |
SNPdbe | rs587780068 |
MSV3d | rs587780068 |
GWAS Ctlg | rs587780068 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780068(T;T) |
Alt | rs587780068(T;T) |
Reference | Rs587780068(C;C) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not specified |
Variation | info |
Gene | TP53 |
CLNDBN | Hereditary cancer-predisposing syndrome not specified |
Reversed | 1 |
HGVS | NC_000017.10:g.7578458G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000115723.8, RCV000213053.1, |