rs11838918
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs11838918(C;C) |
Make rs11838918(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 78836439 |
Gene | LINC00331 |
is a | snp |
is | mentioned by |
dbSNP | rs11838918 |
dbSNP (classic) | rs11838918 |
ClinGen | rs11838918 |
ebi | rs11838918 |
HLI | rs11838918 |
Exac | rs11838918 |
Gnomad | rs11838918 |
Varsome | rs11838918 |
LitVar | rs11838918 |
Map | rs11838918 |
PheGenI | rs11838918 |
Biobank | rs11838918 |
1000 genomes | rs11838918 |
hgdp | rs11838918 |
ensembl | rs11838918 |
geneview | rs11838918 |
scholar | rs11838918 |
rs11838918 | |
pharmgkb | rs11838918 |
gwascentral | rs11838918 |
openSNP | rs11838918 |
23andMe | rs11838918 |
SNPshot | rs11838918 |
SNPdbe | rs11838918 |
MSV3d | rs11838918 |
GWAS Ctlg | rs11838918 |
GMAF | 0.01607 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20585324![]() |
Trait | Conduct disorder (case status) |
Title | Genome-wide association study of conduct disorder symptomatology |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | 2.26 [1.61-3.18] |