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rs17277986

From SNPedia

Orientationplus
Stabilizedplus
Make rs17277986(C;C)
Make rs17277986(C;T)
Make rs17277986(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position106998968
GeneSORCS1
is asnp
is mentioned by
dbSNPrs17277986
ebirs17277986
HLIrs17277986
Exacrs17277986
Varsomers17277986
Maprs17277986
PheGenIrs17277986
hapmaprs17277986
1000 genomesrs17277986
hgdprs17277986
ensemblrs17277986
gopubmedrs17277986
geneviewrs17277986
scholarrs17277986
googlers17277986
pharmgkbrs17277986
gwascentralrs17277986
openSNPrs17277986
23andMers17277986
23andMe allrs17277986
SNP Nexus

SNPshotrs17277986
SNPdbers17277986
MSV3drs17277986
GWAS Ctlgrs17277986
GMAF0.1827
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23279143] Sortilin-related VPS10 domain containing receptor 1 and Alzheimer's disease-associated allelic variations preferentially exist in female or type 2 diabetes mellitus patients in southern Han Chinese

[PMID 23700427OA-icon.png] The Genetic Variation of SORCS1 Is Associated with Late-Onset Alzheimer's Disease in Chinese Han Population [PMID 19241460OA-icon.png] Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10.


[PMID 22353753] SORCS1 and APOE polymorphisms interact to confer risk for late-onset Alzheimer's disease in a Northern Han Chinese population.