rs11575996
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs11575996(A;A) |
Make rs11575996(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 7673535 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs11575996 |
dbSNP (classic) | rs11575996 |
ClinGen | rs11575996 |
ebi | rs11575996 |
HLI | rs11575996 |
Exac | rs11575996 |
Gnomad | rs11575996 |
Varsome | rs11575996 |
LitVar | rs11575996 |
Map | rs11575996 |
PheGenI | rs11575996 |
Biobank | rs11575996 |
1000 genomes | rs11575996 |
hgdp | rs11575996 |
ensembl | rs11575996 |
geneview | rs11575996 |
scholar | rs11575996 |
rs11575996 | |
pharmgkb | rs11575996 |
gwascentral | rs11575996 |
openSNP | rs11575996 |
23andMe | rs11575996 |
SNPshot | rs11575996 |
SNPdbe | rs11575996 |
MSV3d | rs11575996 |
GWAS Ctlg | rs11575996 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs11575996(A;A) rs11575996(T;T) |
Alt | rs11575996(A;A) rs11575996(T;T) |
Reference | Rs11575996(G;G) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | TP53 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.7576853C>T |
CLNSRC | |
CLNACC | RCV000492456.1, |