rs11575997
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 7 | Li-Fraumeni Syndrome (predicted) |
(C;G) | 7 | Li-Fraumeni Syndrome (predicted) |
(G;G) | 0 | common in clinvar |
Make rs11575997(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 7673534 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs11575997 |
dbSNP (classic) | rs11575997 |
ClinGen | rs11575997 |
ebi | rs11575997 |
HLI | rs11575997 |
Exac | rs11575997 |
Gnomad | rs11575997 |
Varsome | rs11575997 |
LitVar | rs11575997 |
Map | rs11575997 |
PheGenI | rs11575997 |
Biobank | rs11575997 |
1000 genomes | rs11575997 |
hgdp | rs11575997 |
ensembl | rs11575997 |
geneview | rs11575997 |
scholar | rs11575997 |
rs11575997 | |
pharmgkb | rs11575997 |
gwascentral | rs11575997 |
openSNP | rs11575997 |
23andMe | rs11575997 |
SNPshot | rs11575997 |
SNPdbe | rs11575997 |
MSV3d | rs11575997 |
GWAS Ctlg | rs11575997 |
Max Magnitude | 7 |
ClinVar | |
---|---|
Risk | rs11575997(C;C) rs11575997(T;T) |
Alt | rs11575997(C;C) rs11575997(T;T) |
Reference | Rs11575997(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TP53 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000017.10:g.7576852C>G |
CLNSRC | |
CLNACC | RCV000429174.1, |