rs3824968
| Orientation | plus |
| Stabilized | plus |
| Make rs3824968(A;A) |
| Make rs3824968(A;T) |
| Make rs3824968(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 121605213 |
| Gene | SORL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3824968 |
| dbSNP (classic) | rs3824968 |
| ClinGen | rs3824968 |
| ebi | rs3824968 |
| HLI | rs3824968 |
| Exac | rs3824968 |
| Gnomad | rs3824968 |
| Varsome | rs3824968 |
| LitVar | rs3824968 |
| Map | rs3824968 |
| PheGenI | rs3824968 |
| Biobank | rs3824968 |
| 1000 genomes | rs3824968 |
| hgdp | rs3824968 |
| ensembl | rs3824968 |
| geneview | rs3824968 |
| scholar | rs3824968 |
| rs3824968 | |
| pharmgkb | rs3824968 |
| gwascentral | rs3824968 |
| openSNP | rs3824968 |
| 23andMe | rs3824968 |
| SNPshot | rs3824968 |
| SNPdbe | rs3824968 |
| MSV3d | rs3824968 |
| GWAS Ctlg | rs3824968 |
| GMAF | 0.3733 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18063222] Alzheimer's disease rs3824968
[PMID 19584446] A study of the SORL1 gene in Alzheimer's disease and cognitive function
[PMID 21997402
] Impact of SORL1 single nucleotide polymorphisms on Alzheimer's disease cerebrospinal fluid markers
[PMID 17826910] Association between genetic variants in sortilin-related receptor 1 (SORL1) and Alzheimer's disease in adults with Down syndrome.
[PMID 18562096] No association of SORL1 SNPs with Alzheimer's disease.
[PMID 18713574] The neuronal sortilin-related receptor gene SORL1 and late-onset Alzheimer's disease.
[PMID 18830724] Assessment of Alzheimer's disease case-control associations using family-based methods.
[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 20574532] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.
[PMID 20625269] Amyloid-beta-Related Genes SORL1 and ACE are Genetically Associated With Risk for Late-onset Alzheimer Disease in the Chinese Population.
[PMID 20667857] Genetic risk factors for cerebral small-vessel disease in hypertensive patients from a genetically isolated population.
[PMID 24083537] SORL1 genetic variants modulate risk of amnestic mild cognitive impairment in northern Han Chinese
[PMID 29865095] Association of sLR11 gene polymorphism with T2DM and carotid atherosclerosis.
