rs587780067
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TG;TG) | 0 | common in clinvar |
Make rs587780067(-;-) |
Make rs587780067(-;TG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 7676003 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs587780067 |
dbSNP (classic) | rs587780067 |
ClinGen | rs587780067 |
ebi | rs587780067 |
HLI | rs587780067 |
Exac | rs587780067 |
Gnomad | rs587780067 |
Varsome | rs587780067 |
LitVar | rs587780067 |
Map | rs587780067 |
PheGenI | rs587780067 |
Biobank | rs587780067 |
1000 genomes | rs587780067 |
hgdp | rs587780067 |
ensembl | rs587780067 |
geneview | rs587780067 |
scholar | rs587780067 |
rs587780067 | |
pharmgkb | rs587780067 |
gwascentral | rs587780067 |
openSNP | rs587780067 |
23andMe | rs587780067 |
SNPshot | rs587780067 |
SNPdbe | rs587780067 |
MSV3d | rs587780067 |
GWAS Ctlg | rs587780067 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780067(-;-) |
Alt | rs587780067(-;-) |
Reference | Rs587780067(TG;TG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TP53 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000017.10:g.7579321_7579322delCA |
CLNSRC | |
CLNACC | RCV000115720.3, |