rs2509382
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2509382(C;C) |
Make rs2509382(C;G) |
Make rs2509382(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 91046275 |
is a | snp |
is | mentioned by |
dbSNP | rs2509382 |
dbSNP (classic) | rs2509382 |
ClinGen | rs2509382 |
ebi | rs2509382 |
HLI | rs2509382 |
Exac | rs2509382 |
Gnomad | rs2509382 |
Varsome | rs2509382 |
LitVar | rs2509382 |
Map | rs2509382 |
PheGenI | rs2509382 |
Biobank | rs2509382 |
1000 genomes | rs2509382 |
hgdp | rs2509382 |
ensembl | rs2509382 |
geneview | rs2509382 |
scholar | rs2509382 |
rs2509382 | |
pharmgkb | rs2509382 |
gwascentral | rs2509382 |
openSNP | rs2509382 |
23andMe | rs2509382 |
SNPshot | rs2509382 |
SNPdbe | rs2509382 |
MSV3d | rs2509382 |
GWAS Ctlg | rs2509382 |
GMAF | 0.1437 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 22891933] Analysis of the DISC1 translocation partner (11q14.3) in genetic risk of schizophrenia
[PMID 25670952] Disrupted-in-Schizophrenia-1 SNPs and Susceptibility to Schizophrenia: Evidence from Malaysia