rs10744743
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10744743(C;C) |
Make rs10744743(C;G) |
Make rs10744743(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 119805261 |
Gene | CIT |
is a | snp |
is | mentioned by |
dbSNP | rs10744743 |
dbSNP (classic) | rs10744743 |
ClinGen | rs10744743 |
ebi | rs10744743 |
HLI | rs10744743 |
Exac | rs10744743 |
Gnomad | rs10744743 |
Varsome | rs10744743 |
LitVar | rs10744743 |
Map | rs10744743 |
PheGenI | rs10744743 |
Biobank | rs10744743 |
1000 genomes | rs10744743 |
hgdp | rs10744743 |
ensembl | rs10744743 |
geneview | rs10744743 |
scholar | rs10744743 |
rs10744743 | |
pharmgkb | rs10744743 |
gwascentral | rs10744743 |
openSNP | rs10744743 |
23andMe | rs10744743 |
SNPshot | rs10744743 |
SNPdbe | rs10744743 |
MSV3d | rs10744743 |
GWAS Ctlg | rs10744743 |
GMAF | 0.3636 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 20084519] Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging