rs876658153
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6.3 | Hereditary cancer predisposing syndrome |
(G;G) | 0 | common in clinvar |
Make rs876658153(G;T) |
Make rs876658153(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 87925558 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs876658153 |
dbSNP (classic) | rs876658153 |
ClinGen | rs876658153 |
ebi | rs876658153 |
HLI | rs876658153 |
Exac | rs876658153 |
Gnomad | rs876658153 |
Varsome | rs876658153 |
LitVar | rs876658153 |
Map | rs876658153 |
PheGenI | rs876658153 |
Biobank | rs876658153 |
1000 genomes | rs876658153 |
hgdp | rs876658153 |
ensembl | rs876658153 |
geneview | rs876658153 |
scholar | rs876658153 |
rs876658153 | |
pharmgkb | rs876658153 |
gwascentral | rs876658153 |
openSNP | rs876658153 |
23andMe | rs876658153 |
SNPshot | rs876658153 |
SNPdbe | rs876658153 |
MSV3d | rs876658153 |
GWAS Ctlg | rs876658153 |
Max Magnitude | 6.3 |
ClinVar | |
---|---|
Risk | rs876658153(A;A) rs876658153(T;T) |
Alt | rs876658153(A;A) rs876658153(T;T) |
Reference | Rs876658153(G;G) |
Significance | Pathogenic |
Disease | not provided Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | PTEN |
CLNDBN | not provided Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.89685315G>A; NC_000010.10:g.89685315G>T |
CLNSRC | |
CLNACC | RCV000482154.1, RCV000491897.1, RCV000213295.1, |