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rs2297660

From SNPedia

Orientationminus
Stabilizedminus
Make rs2297660(A;A)
Make rs2297660(A;C)
Make rs2297660(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position53266643
GeneLOC105378728, LRP8
is asnp
is mentioned by
dbSNPrs2297660
dbSNP (classic)rs2297660
ClinGenrs2297660
ebirs2297660
HLIrs2297660
Exacrs2297660
Gnomadrs2297660
Varsomers2297660
LitVarrs2297660
Maprs2297660
PheGenIrs2297660
Biobankrs2297660
1000 genomesrs2297660
hgdprs2297660
ensemblrs2297660
geneviewrs2297660
scholarrs2297660
googlers2297660
pharmgkbrs2297660
gwascentralrs2297660
openSNPrs2297660
23andMers2297660
SNPshotrs2297660
SNPdbers2297660
MSV3drs2297660
GWAS Ctlgrs2297660
GMAF0.4017
Max Magnitude0
? (A;A) (A;C) (C;C) 28


OMIM602600
DescLOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 8; LRP8
Variant
Relatedalso



[PMID 22419519] Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia.



[PMID 23524007OA-icon.png] Multi-allelic haplotype association identifies novel information different from single-SNP analysis: a new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI.


[PMID 24867879OA-icon.png] A Novel Molecular Diagnostic Marker for Familial and Early-Onset CAD and MI in the LRP8 Gene


[PMID 29032149] TG haplotype in the LRP8 is associated with myocardial infarction in south Indian population.