rs28694718
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 1.5 | >2x higher risk for schizophrenia |
(A;G) | 1.5 | 2x higher risk for schizophrenia |
(G;G) | common |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 1295332 |
Gene | CSF2RA |
is a | snp |
is | mentioned by |
dbSNP | rs28694718 |
dbSNP (classic) | rs28694718 |
ClinGen | rs28694718 |
ebi | rs28694718 |
HLI | rs28694718 |
Exac | rs28694718 |
Gnomad | rs28694718 |
Varsome | rs28694718 |
LitVar | rs28694718 |
Map | rs28694718 |
PheGenI | rs28694718 |
Biobank | rs28694718 |
1000 genomes | rs28694718 |
hgdp | rs28694718 |
ensembl | rs28694718 |
geneview | rs28694718 |
scholar | rs28694718 |
rs28694718 | |
pharmgkb | rs28694718 |
gwascentral | rs28694718 |
openSNP | rs28694718 |
23andMe | rs28694718 |
SNPshot | rs28694718 |
SNPdbe | rs28694718 |
MSV3d | rs28694718 |
GWAS Ctlg | rs28694718 |
GMAF | 0.2773 |
Max Magnitude | 1.5 |
In the Pseudoautosomal region
rs28694718, located in intron 8 of the CSF2RA gene, is part of a haplotype block that has been reported in a whole genome association study to be associated with schizophrenia. (The other SNP in this block is rs28414810.)
The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with this allele is 2.11. [PMID 17522711]