rs193920789
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;T) | 7 | Li-Fraumeni Syndrome (predicted) |
(T;T) | 0 | common in clinvar |
Make rs193920789(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 7674249 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs193920789 |
dbSNP (classic) | rs193920789 |
ClinGen | rs193920789 |
ebi | rs193920789 |
HLI | rs193920789 |
Exac | rs193920789 |
Gnomad | rs193920789 |
Varsome | rs193920789 |
LitVar | rs193920789 |
Map | rs193920789 |
PheGenI | rs193920789 |
Biobank | rs193920789 |
1000 genomes | rs193920789 |
hgdp | rs193920789 |
ensembl | rs193920789 |
geneview | rs193920789 |
scholar | rs193920789 |
rs193920789 | |
pharmgkb | rs193920789 |
gwascentral | rs193920789 |
openSNP | rs193920789 |
23andMe | rs193920789 |
SNPshot | rs193920789 |
SNPdbe | rs193920789 |
MSV3d | rs193920789 |
GWAS Ctlg | rs193920789 |
Max Magnitude | 7 |
ClinVar | |
---|---|
Risk | rs193920789(G;G) |
Alt | rs193920789(G;G) |
Reference | Rs193920789(T;T) |
Significance | Pathogenic |
Disease | Malignant tumor of prostate Li-Fraumeni syndrome |
Variation | info |
Gene | TP53 |
CLNDBN | Malignant tumor of prostate Li-Fraumeni syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.7577567A>C |
CLNSRC | |
CLNACC | RCV000149049.1, RCV000203823.1, |