rs151222
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common on affy axiom data |
Make rs151222(C;C) |
Make rs151222(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 20663170 |
Gene | ACSM1 |
is a | snp |
is | mentioned by |
dbSNP | rs151222 |
dbSNP (classic) | rs151222 |
ClinGen | rs151222 |
ebi | rs151222 |
HLI | rs151222 |
Exac | rs151222 |
Gnomad | rs151222 |
Varsome | rs151222 |
LitVar | rs151222 |
Map | rs151222 |
PheGenI | rs151222 |
Biobank | rs151222 |
1000 genomes | rs151222 |
hgdp | rs151222 |
ensembl | rs151222 |
geneview | rs151222 |
scholar | rs151222 |
rs151222 | |
pharmgkb | rs151222 |
gwascentral | rs151222 |
openSNP | rs151222 |
23andMe | rs151222 |
SNPshot | rs151222 |
SNPdbe | rs151222 |
MSV3d | rs151222 |
GWAS Ctlg | rs151222 |
GMAF | 0.09045 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs151222 |
PubMedID | [PMID 18347602] |
Condition | Schizophrenia |
Gene | ACSM1, BUCS1 |
Risk Allele | |
pValue | 6.00E-006 |
OR | 2.1 |
95% CI |
[PMID 19197363] A genome-wide investigation of SNPs and CNVs in schizophrenia.