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rs3820198

From SNPedia

Orientationminus
Stabilizedminus
Make rs3820198(G;G)
Make rs3820198(G;T)
Make rs3820198(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position53326979
GeneLRP8
is asnp
is mentioned by
dbSNPrs3820198
ebirs3820198
HLIrs3820198
Exacrs3820198
Varsomers3820198
Maprs3820198
PheGenIrs3820198
hapmaprs3820198
1000 genomesrs3820198
hgdprs3820198
ensemblrs3820198
gopubmedrs3820198
geneviewrs3820198
scholarrs3820198
googlers3820198
pharmgkbrs3820198
gwascentralrs3820198
openSNPrs3820198
23andMers3820198
23andMe allrs3820198
SNP Nexus

SNPshotrs3820198
SNPdbers3820198
MSV3drs3820198
GWAS Ctlgrs3820198
GMAF0.4789
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 21316997] Investigation of LRP8 gene in 1p31 QTL linked to LDL peak particle diameter in the Quebec family study


[PMID 17847002OA-icon.png] An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.


GET Evidence
LRP8-D46E
aa_change Asp46Glu
aa_change_short D46E
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.522867
summary



[PMID 22889673] Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population.