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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
GeneLRP8
is asnp
is mentioned by
dbSNPrs2297660
ebirs2297660
HLIrs2297660
Exacrs2297660
Varsomers2297660
Maprs2297660
PheGenIrs2297660
hapmaprs2297660
1000 genomesrs2297660
hgdprs2297660
ensemblrs2297660
gopubmedrs2297660
geneviewrs2297660
scholarrs2297660
googlers2297660
pharmgkbrs2297660
gwascentralrs2297660
openSNPrs2297660
23andMers2297660
23andMe allrs2297660
SNP Nexus

SNPshotrs2297660
SNPdbers2297660
MSV3drs2297660
GWAS Ctlgrs2297660
GMAF0.4017
Max Magnitude
? (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.


GET Evidence
rs2297660
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.345138
summary



[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