rs1057517840
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GA;GA) | 0 | common in clinvar |
Make rs1057517840(-;-) |
Make rs1057517840(-;GA) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 7674904 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs1057517840 |
dbSNP (classic) | rs1057517840 |
ClinGen | rs1057517840 |
ebi | rs1057517840 |
HLI | rs1057517840 |
Exac | rs1057517840 |
Gnomad | rs1057517840 |
Varsome | rs1057517840 |
LitVar | rs1057517840 |
Map | rs1057517840 |
PheGenI | rs1057517840 |
Biobank | rs1057517840 |
1000 genomes | rs1057517840 |
hgdp | rs1057517840 |
ensembl | rs1057517840 |
geneview | rs1057517840 |
scholar | rs1057517840 |
rs1057517840 | |
pharmgkb | rs1057517840 |
gwascentral | rs1057517840 |
openSNP | rs1057517840 |
23andMe | rs1057517840 |
SNPshot | rs1057517840 |
SNPdbe | rs1057517840 |
MSV3d | rs1057517840 |
GWAS Ctlg | rs1057517840 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057517840(-;-) |
Alt | rs1057517840(-;-) |
Reference | Rs1057517840(GA;GA) |
Significance | Pathogenic |
Disease | not provided Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | TP53 |
CLNDBN | not provided Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.7578222_7578223delTC |
CLNSRC | |
CLNACC | RCV000414120.1, RCV000492427.1, |