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rs1799986

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs1799986(C;T)
Make rs1799986(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position57141483
GeneLRP1
is asnp
is mentioned by
dbSNPrs1799986
dbSNP (classic)rs1799986
ClinGenrs1799986
ebirs1799986
HLIrs1799986
Exacrs1799986
Gnomadrs1799986
Varsomers1799986
LitVarrs1799986
Maprs1799986
PheGenIrs1799986
Biobankrs1799986
1000 genomesrs1799986
hgdprs1799986
ensemblrs1799986
geneviewrs1799986
scholarrs1799986
googlers1799986
pharmgkbrs1799986
gwascentralrs1799986
openSNPrs1799986
23andMers1799986
SNPshotrs1799986
SNPdbers1799986
MSV3drs1799986
GWAS Ctlgrs1799986
GMAF0.1047
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19684401] Genetic Interaction between Tau and the Apolipoprotein E Receptor LRP1 Increases Alzheimer's Disease Risk


[PMID 17517621OA-icon.png] Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease.


[PMID 19105203OA-icon.png] An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.


[PMID 23186781] Association of polymorphisms in the LRP1 and A2M genes with Alzheimer's disease in the Northern Chinese Han population


[PMID 23404896OA-icon.png] Low density lipoprotein receptor related protein 1 variant interacts with saturated fatty acids in Puerto Ricans


[PMID 22819221] LRP1 gene polymorphisms are associated with premature risk of cardiovascular disease in patients with familial hypercholesterolemia.


[PMID 31560818OA-icon.png] Variations of Wnt/β-catenin pathway-related genes in susceptibility to knee osteoarthritis: A three-centre case-control study.