rs587782345
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs587782345(A;G) |
Make rs587782345(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 87965326 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs587782345 |
dbSNP (classic) | rs587782345 |
ClinGen | rs587782345 |
ebi | rs587782345 |
HLI | rs587782345 |
Exac | rs587782345 |
Gnomad | rs587782345 |
Varsome | rs587782345 |
LitVar | rs587782345 |
Map | rs587782345 |
PheGenI | rs587782345 |
Biobank | rs587782345 |
1000 genomes | rs587782345 |
hgdp | rs587782345 |
ensembl | rs587782345 |
geneview | rs587782345 |
scholar | rs587782345 |
rs587782345 | |
pharmgkb | rs587782345 |
gwascentral | rs587782345 |
openSNP | rs587782345 |
23andMe | rs587782345 |
SNPshot | rs587782345 |
SNPdbe | rs587782345 |
MSV3d | rs587782345 |
GWAS Ctlg | rs587782345 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782345(C;C) rs587782345(G;G) rs587782345(T;T) |
Alt | rs587782345(C;C) rs587782345(G;G) rs587782345(T;T) |
Reference | Rs587782345(A;A) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome not specified |
Variation | info |
Gene | PTEN |
CLNDBN | Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome not specified |
Reversed | 0 |
HGVS | NC_000010.10:g.89725083A>G; NC_000010.10:g.89725083A>T |
CLNSRC | |
CLNACC | RCV000131284.2, RCV000463640.1, RCV000169786.2, RCV000456755.1, |