rs289585
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs289585(A;A) |
Make rs289585(A;G) |
Make rs289585(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 13403027 |
Gene | DLC1 |
is a | snp |
is | mentioned by |
dbSNP | rs289585 |
dbSNP (classic) | rs289585 |
ClinGen | rs289585 |
ebi | rs289585 |
HLI | rs289585 |
Exac | rs289585 |
Gnomad | rs289585 |
Varsome | rs289585 |
LitVar | rs289585 |
Map | rs289585 |
PheGenI | rs289585 |
Biobank | rs289585 |
1000 genomes | rs289585 |
hgdp | rs289585 |
ensembl | rs289585 |
geneview | rs289585 |
scholar | rs289585 |
rs289585 | |
pharmgkb | rs289585 |
gwascentral | rs289585 |
openSNP | rs289585 |
23andMe | rs289585 |
SNPshot | rs289585 |
SNPdbe | rs289585 |
MSV3d | rs289585 |
GWAS Ctlg | rs289585 |
GMAF | 0.101 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22688191] |
Trait | |
Title | Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. |
Risk Allele | |
P-val | 0.000005 |
Odds Ratio | 1.4500 None |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 8
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d