rs10503256
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10503256(A;A) |
Make rs10503256(A;G) |
Make rs10503256(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 4356657 |
Gene | CSMD1 |
is a | snp |
is | mentioned by |
dbSNP | rs10503256 |
dbSNP (classic) | rs10503256 |
ClinGen | rs10503256 |
ebi | rs10503256 |
HLI | rs10503256 |
Exac | rs10503256 |
Gnomad | rs10503256 |
Varsome | rs10503256 |
LitVar | rs10503256 |
Map | rs10503256 |
PheGenI | rs10503256 |
Biobank | rs10503256 |
1000 genomes | rs10503256 |
hgdp | rs10503256 |
ensembl | rs10503256 |
geneview | rs10503256 |
scholar | rs10503256 |
rs10503256 | |
pharmgkb | rs10503256 |
gwascentral | rs10503256 |
openSNP | rs10503256 |
23andMe | rs10503256 |
SNPshot | rs10503256 |
SNPdbe | rs10503256 |
MSV3d | rs10503256 |
GWAS Ctlg | rs10503256 |
GMAF | 0.4178 |
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 | 9E-7 |
Odds Ratio | 1.1000 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 FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d