rs1699102
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1699102(C;C) |
| Make rs1699102(C;T) |
| Make rs1699102(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 121586253 |
| Gene | SORL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1699102 |
| dbSNP (classic) | rs1699102 |
| ClinGen | rs1699102 |
| ebi | rs1699102 |
| HLI | rs1699102 |
| Exac | rs1699102 |
| Gnomad | rs1699102 |
| Varsome | rs1699102 |
| LitVar | rs1699102 |
| Map | rs1699102 |
| PheGenI | rs1699102 |
| Biobank | rs1699102 |
| 1000 genomes | rs1699102 |
| hgdp | rs1699102 |
| ensembl | rs1699102 |
| geneview | rs1699102 |
| scholar | rs1699102 |
| rs1699102 | |
| pharmgkb | rs1699102 |
| gwascentral | rs1699102 |
| openSNP | rs1699102 |
| 23andMe | rs1699102 |
| SNPshot | rs1699102 |
| SNPdbe | rs1699102 |
| MSV3d | rs1699102 |
| GWAS Ctlg | rs1699102 |
| GMAF | 0.4541 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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[PMID 18063222] SORL1 haplotypes modulate risk of Alzheimer's disease in Chinese
[PMID 19584446] A study of the SORL1 gene in Alzheimer's disease and cognitive function
[PMID 17826910
] Association between genetic variants in sortilin-related receptor 1 (SORL1) and Alzheimer's disease in adults with Down syndrome.
[PMID 18938222] Allelic mRNA expression of sortilin-1 (SORL1) mRNA in Alzheimer's autopsy brain tissues.
[PMID 19064752] Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease.
[PMID 20667857] Genetic risk factors for cerebral small-vessel disease in hypertensive patients from a genetically isolated population.
