rs2297660
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2297660(A;A) |
Make rs2297660(A;C) |
Make rs2297660(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 53266643 |
Gene | LOC105378728, LRP8 |
is a | snp |
is | mentioned by |
dbSNP | rs2297660 |
dbSNP (classic) | rs2297660 |
ClinGen | rs2297660 |
ebi | rs2297660 |
HLI | rs2297660 |
Exac | rs2297660 |
Gnomad | rs2297660 |
Varsome | rs2297660 |
LitVar | rs2297660 |
Map | rs2297660 |
PheGenI | rs2297660 |
Biobank | rs2297660 |
1000 genomes | rs2297660 |
hgdp | rs2297660 |
ensembl | rs2297660 |
geneview | rs2297660 |
scholar | rs2297660 |
rs2297660 | |
pharmgkb | rs2297660 |
gwascentral | rs2297660 |
openSNP | rs2297660 |
23andMe | rs2297660 |
SNPshot | rs2297660 |
SNPdbe | rs2297660 |
MSV3d | rs2297660 |
GWAS Ctlg | rs2297660 |
GMAF | 0.4017 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 22419519] Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia.
[PMID 23524007] 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 24867879] 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.