rs786202082
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;C) | 7 | Li-Fraumeni Syndrome (predicted) |
(C;C) | 0 | common in clinvar |
(C;G) | 7 | Li-Fraumeni Syndrome (predicted) |
Make rs786202082(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 7673793 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs786202082 |
dbSNP (classic) | rs786202082 |
ClinGen | rs786202082 |
ebi | rs786202082 |
HLI | rs786202082 |
Exac | rs786202082 |
Gnomad | rs786202082 |
Varsome | rs786202082 |
LitVar | rs786202082 |
Map | rs786202082 |
PheGenI | rs786202082 |
Biobank | rs786202082 |
1000 genomes | rs786202082 |
hgdp | rs786202082 |
ensembl | rs786202082 |
geneview | rs786202082 |
scholar | rs786202082 |
rs786202082 | |
pharmgkb | rs786202082 |
gwascentral | rs786202082 |
openSNP | rs786202082 |
23andMe | rs786202082 |
SNPshot | rs786202082 |
SNPdbe | rs786202082 |
MSV3d | rs786202082 |
GWAS Ctlg | rs786202082 |
Max Magnitude | 7 |
ClinVar | |
---|---|
Risk | rs786202082(A;A) rs786202082(G;G) |
Alt | rs786202082(A;A) rs786202082(G;G) |
Reference | Rs786202082(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | TP53 |
CLNDBN | Hereditary cancer-predisposing syndrome not provided |
Reversed | 1 |
HGVS | NC_000017.10:g.7577111G>C; NC_000017.10:g.7577111G>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000164718.2, RCV000223364.1, RCV000236401.1, |