rs587782596
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587782596(C;T) |
Make rs587782596(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 7675071 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs587782596 |
dbSNP (classic) | rs587782596 |
ClinGen | rs587782596 |
ebi | rs587782596 |
HLI | rs587782596 |
Exac | rs587782596 |
Gnomad | rs587782596 |
Varsome | rs587782596 |
LitVar | rs587782596 |
Map | rs587782596 |
PheGenI | rs587782596 |
Biobank | rs587782596 |
1000 genomes | rs587782596 |
hgdp | rs587782596 |
ensembl | rs587782596 |
geneview | rs587782596 |
scholar | rs587782596 |
rs587782596 | |
pharmgkb | rs587782596 |
gwascentral | rs587782596 |
openSNP | rs587782596 |
23andMe | rs587782596 |
SNPshot | rs587782596 |
SNPdbe | rs587782596 |
MSV3d | rs587782596 |
GWAS Ctlg | rs587782596 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782596(A;A) rs587782596(T;T) |
Alt | rs587782596(A;A) rs587782596(T;T) |
Reference | Rs587782596(C;C) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not specified |
Variation | info |
Gene | TP53 |
CLNDBN | Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome not specified |
Reversed | 1 |
HGVS | NC_000017.10:g.7578389G>A; NC_000017.10:g.7578389G>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000131943.4, RCV000168292.1, RCV000236276.1, RCV000222957.1, |