rs1085308047
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Chromosome | 10 |
| Position | 87864509 |
| Gene | KLLN, PTEN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1085308047 |
| dbSNP (classic) | rs1085308047 |
| ClinGen | rs1085308047 |
| ebi | rs1085308047 |
| HLI | rs1085308047 |
| Exac | rs1085308047 |
| Gnomad | rs1085308047 |
| Varsome | rs1085308047 |
| LitVar | rs1085308047 |
| Map | rs1085308047 |
| PheGenI | rs1085308047 |
| Biobank | rs1085308047 |
| 1000 genomes | rs1085308047 |
| hgdp | rs1085308047 |
| ensembl | rs1085308047 |
| geneview | rs1085308047 |
| scholar | rs1085308047 |
| rs1085308047 | |
| pharmgkb | rs1085308047 |
| gwascentral | rs1085308047 |
| openSNP | rs1085308047 |
| 23andMe | rs1085308047 |
| SNPshot | rs1085308047 |
| SNPdbe | rs1085308047 |
| MSV3d | rs1085308047 |
| GWAS Ctlg | rs1085308047 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1085308047(G;G) |
| Alt | rs1085308047(G;G) |
| Reference | Rs1085308047(A;A) |
| Significance | Pathogenic |
| Disease | PTEN hamartoma tumor syndrome not provided |
| Variation | info |
| Gene | PTEN KLLN |
| CLNDBN | PTEN hamartoma tumor syndrome not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.89624266A>G |
| CLNSRC | |
| CLNACC | RCV000490585.1, RCV000492940.1, |
