rs10884399
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10884399(A;A) |
| Make rs10884399(A;G) |
| Make rs10884399(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 107013177 |
| Gene | SORCS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10884399 |
| dbSNP (classic) | rs10884399 |
| ClinGen | rs10884399 |
| ebi | rs10884399 |
| HLI | rs10884399 |
| Exac | rs10884399 |
| Gnomad | rs10884399 |
| Varsome | rs10884399 |
| LitVar | rs10884399 |
| Map | rs10884399 |
| PheGenI | rs10884399 |
| Biobank | rs10884399 |
| 1000 genomes | rs10884399 |
| hgdp | rs10884399 |
| ensembl | rs10884399 |
| geneview | rs10884399 |
| scholar | rs10884399 |
| rs10884399 | |
| pharmgkb | rs10884399 |
| gwascentral | rs10884399 |
| openSNP | rs10884399 |
| 23andMe | rs10884399 |
| SNPshot | rs10884399 |
| SNPdbe | rs10884399 |
| MSV3d | rs10884399 |
| GWAS Ctlg | rs10884399 |
| GMAF | 0.2424 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23279143] Sortilin-related VPS10 domain containing receptor 1 and Alzheimer's disease-associated allelic variations preferentially exist in female or type 2 diabetes mellitus patients in southern Han Chinese
[PMID 19241460
] Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10.
