rs878853933
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;C) | 6.3 | PTEN hamartoma tumor syndrome |
Make rs878853933(C;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 87894077 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs878853933 |
dbSNP (classic) | rs878853933 |
ClinGen | rs878853933 |
ebi | rs878853933 |
HLI | rs878853933 |
Exac | rs878853933 |
Gnomad | rs878853933 |
Varsome | rs878853933 |
LitVar | rs878853933 |
Map | rs878853933 |
PheGenI | rs878853933 |
Biobank | rs878853933 |
1000 genomes | rs878853933 |
hgdp | rs878853933 |
ensembl | rs878853933 |
geneview | rs878853933 |
scholar | rs878853933 |
rs878853933 | |
pharmgkb | rs878853933 |
gwascentral | rs878853933 |
openSNP | rs878853933 |
23andMe | rs878853933 |
SNPshot | rs878853933 |
SNPdbe | rs878853933 |
MSV3d | rs878853933 |
GWAS Ctlg | rs878853933 |
Max Magnitude | 6.3 |
ClinVar | |
---|---|
Risk | rs878853933(C;C) |
Alt | rs878853933(C;C) |
Reference | Rs878853933(-;-) |
Significance | Pathogenic |
Disease | PTEN hamartoma tumor syndrome |
Variation | info |
Gene | PTEN |
CLNDBN | PTEN hamartoma tumor syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.89653834dupC |
CLNSRC | |
CLNACC | RCV000226096.1, |