rs115329265
From SNPedia
Merged into | rs1233578 |
Orientation | plus |
Stabilized | plus |
Make rs115329265(A;A) |
Make rs115329265(A;G) |
Make rs115329265(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 28744470 |
is a | snp |
is | mentioned by |
dbSNP | rs115329265 |
dbSNP (classic) | rs115329265 |
ClinGen | rs115329265 |
ebi | rs115329265 |
HLI | rs115329265 |
Exac | rs115329265 |
Gnomad | rs115329265 |
Varsome | rs115329265 |
LitVar | rs115329265 |
Map | rs115329265 |
PheGenI | rs115329265 |
Biobank | rs115329265 |
1000 genomes | rs115329265 |
hgdp | rs115329265 |
ensembl | rs115329265 |
geneview | rs115329265 |
scholar | rs115329265 |
rs115329265 | |
pharmgkb | rs115329265 |
gwascentral | rs115329265 |
openSNP | rs115329265 |
23andMe | rs115329265 |
SNPshot | rs115329265 |
SNPdbe | rs115329265 |
MSV3d | rs115329265 |
GWAS Ctlg | rs115329265 |
Status | Merged into rs1233578 |
Max Magnitude | 0 |
A study ranked this SNP first in terms of evidence from p value for schizophrenia risk.
The A allele is reference (G allele is risk) OR=1.205(95 CI 1.168-1.244) p= 3.48e-31.