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rs3824968

From SNPedia

Orientationplus
Stabilizedplus
Make rs3824968(A;A)
Make rs3824968(A;T)
Make rs3824968(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position121605213
GeneSORL1
is asnp
is mentioned by
dbSNPrs3824968
ebirs3824968
HLIrs3824968
Exacrs3824968
Varsomers3824968
Maprs3824968
PheGenIrs3824968
hapmaprs3824968
1000 genomesrs3824968
hgdprs3824968
ensemblrs3824968
gopubmedrs3824968
geneviewrs3824968
scholarrs3824968
googlers3824968
pharmgkbrs3824968
gwascentralrs3824968
openSNPrs3824968
23andMers3824968
23andMe allrs3824968
SNP Nexus

SNPshotrs3824968
SNPdbers3824968
MSV3drs3824968
GWAS Ctlgrs3824968
GMAF0.3733
Max Magnitude
? (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 21997402OA-icon.png] Impact of SORL1 single nucleotide polymorphisms on Alzheimer's disease cerebrospinal fluid markers

[PMID 17826910OA-icon.png] Association between genetic variants in sortilin-related receptor 1 (SORL1) and Alzheimer's disease in adults with Down syndrome.

[PMID 18562096OA-icon.png] No association of SORL1 SNPs with Alzheimer's disease.

[PMID 18713574OA-icon.png] The neuronal sortilin-related receptor gene SORL1 and late-onset Alzheimer's disease.

[PMID 18830724OA-icon.png] Assessment of Alzheimer's disease case-control associations using family-based methods.

[PMID 18938222OA-icon.png] Allelic mRNA expression of sortilin-1 (SORL1) mRNA in Alzheimer's autopsy brain tissues.

[PMID 19064752OA-icon.png] Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease.

[PMID 19362127OA-icon.png] Endophenotypes in normal brain morphology and Alzheimer's disease: a review.

[PMID 19368828] Association of SORL1 gene variants with Alzheimer's disease.

[PMID 19906263OA-icon.png] Use of genetic variation as biomarkers for Alzheimer's disease.

[PMID 20061642OA-icon.png] Use of genetic variation as biomarkers for mild cognitive impairment and progression of mild cognitive impairment to dementia.

[PMID 20574532OA-icon.png] 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