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rs1699102

From SNPedia

Orientationplus
Stabilizedplus
Make rs1699102(C;C)
Make rs1699102(C;T)
Make rs1699102(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position121586253
GeneSORL1
is asnp
is mentioned by
dbSNPrs1699102
ebirs1699102
HLIrs1699102
Exacrs1699102
Varsomers1699102
Maprs1699102
PheGenIrs1699102
hapmaprs1699102
1000 genomesrs1699102
hgdprs1699102
ensemblrs1699102
gopubmedrs1699102
geneviewrs1699102
scholarrs1699102
googlers1699102
pharmgkbrs1699102
gwascentralrs1699102
openSNPrs1699102
23andMers1699102
23andMe allrs1699102
SNP Nexus

SNPshotrs1699102
SNPdbers1699102
MSV3drs1699102
GWAS Ctlgrs1699102
GMAF0.4541
Max Magnitude
? (C;C) (C;T) (T;T) 28

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


[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 20667857] Genetic risk factors for cerebral small-vessel disease in hypertensive patients from a genetically isolated population.