rs1010159
| Orientation | minus |
| Stabilized | minus |
| Make rs1010159(A;A) |
| Make rs1010159(A;G) |
| Make rs1010159(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 121612692 |
| Gene | SORL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1010159 |
| dbSNP (classic) | rs1010159 |
| ClinGen | rs1010159 |
| ebi | rs1010159 |
| HLI | rs1010159 |
| Exac | rs1010159 |
| Gnomad | rs1010159 |
| Varsome | rs1010159 |
| LitVar | rs1010159 |
| Map | rs1010159 |
| PheGenI | rs1010159 |
| Biobank | rs1010159 |
| 1000 genomes | rs1010159 |
| hgdp | rs1010159 |
| ensembl | rs1010159 |
| geneview | rs1010159 |
| scholar | rs1010159 |
| rs1010159 | |
| pharmgkb | rs1010159 |
| gwascentral | rs1010159 |
| openSNP | rs1010159 |
| 23andMe | rs1010159 |
| SNPshot | rs1010159 |
| SNPdbe | rs1010159 |
| MSV3d | rs1010159 |
| GWAS Ctlg | rs1010159 |
| GMAF | 0.4876 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[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 17903297] Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.
[PMID 18713574] The neuronal sortilin-related receptor gene SORL1 and late-onset Alzheimer's disease.
[PMID 18813964] Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid beta.
[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 19362127] Endophenotypes in normal brain morphology and Alzheimer's disease: a review.
[PMID 19368828] Association of SORL1 gene variants with Alzheimer's disease.
[PMID 19906263] Use of genetic variation as biomarkers for Alzheimer's disease.
[PMID 20061642] Use of genetic variation as biomarkers for mild cognitive impairment and progression of mild cognitive impairment to dementia.
[PMID 20667857] Genetic risk factors for cerebral small-vessel disease in hypertensive patients from a genetically isolated population.
[PMID 26611835] Meta-analysis of the Association between Alzheimer Disease and Variants in GAB2, PICALM, and SORL1.
