rs8179116
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs8179116(A;A) |
Make rs8179116(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 108631651 |
Gene | LOC105369968, SELPLG |
is a | snp |
is | mentioned by |
dbSNP | rs8179116 |
dbSNP (classic) | rs8179116 |
ClinGen | rs8179116 |
ebi | rs8179116 |
HLI | rs8179116 |
Exac | rs8179116 |
Gnomad | rs8179116 |
Varsome | rs8179116 |
LitVar | rs8179116 |
Map | rs8179116 |
PheGenI | rs8179116 |
Biobank | rs8179116 |
1000 genomes | rs8179116 |
hgdp | rs8179116 |
ensembl | rs8179116 |
geneview | rs8179116 |
scholar | rs8179116 |
rs8179116 | |
pharmgkb | rs8179116 |
gwascentral | rs8179116 |
openSNP | rs8179116 |
23andMe | rs8179116 |
SNPshot | rs8179116 |
SNPdbe | rs8179116 |
MSV3d | rs8179116 |
GWAS Ctlg | rs8179116 |
GMAF | 0.02296 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20585324] |
Trait | Conduct disorder (symptom count) |
Title | Genome-wide association study of conduct disorder symptomatology |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | 0.23 [NR] unit increase |