rs729397
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs729397(C;C) |
Make rs729397(C;G) |
Make rs729397(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 2489827 |
Gene | LOC105376351 |
is a | snp |
is | mentioned by |
dbSNP | rs729397 |
dbSNP (classic) | rs729397 |
ClinGen | rs729397 |
ebi | rs729397 |
HLI | rs729397 |
Exac | rs729397 |
Gnomad | rs729397 |
Varsome | rs729397 |
LitVar | rs729397 |
Map | rs729397 |
PheGenI | rs729397 |
Biobank | rs729397 |
1000 genomes | rs729397 |
hgdp | rs729397 |
ensembl | rs729397 |
geneview | rs729397 |
scholar | rs729397 |
rs729397 | |
pharmgkb | rs729397 |
gwascentral | rs729397 |
openSNP | rs729397 |
23andMe | rs729397 |
SNPshot | rs729397 |
SNPdbe | rs729397 |
MSV3d | rs729397 |
GWAS Ctlg | rs729397 |
GMAF | 0.2245 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20339536![]() |
Trait | Response to statin therapy |
Title | Genome-wide association of lipid-lowering response to statins in combined study populations |
Risk Allele | C |
P-val | 0.000008 |
Odds Ratio | None None |
[PMID 16400611] Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.