rs2720508
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs2720508(C;C) |
Make rs2720508(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 17472318 |
Gene | ADAM24P |
is a | snp |
is | mentioned by |
dbSNP | rs2720508 |
dbSNP (classic) | rs2720508 |
ClinGen | rs2720508 |
ebi | rs2720508 |
HLI | rs2720508 |
Exac | rs2720508 |
Gnomad | rs2720508 |
Varsome | rs2720508 |
LitVar | rs2720508 |
Map | rs2720508 |
PheGenI | rs2720508 |
Biobank | rs2720508 |
1000 genomes | rs2720508 |
hgdp | rs2720508 |
ensembl | rs2720508 |
geneview | rs2720508 |
scholar | rs2720508 |
rs2720508 | |
pharmgkb | rs2720508 |
gwascentral | rs2720508 |
openSNP | rs2720508 |
23andMe | rs2720508 |
SNPshot | rs2720508 |
SNPdbe | rs2720508 |
MSV3d | rs2720508 |
GWAS Ctlg | rs2720508 |
GMAF | 0.08264 |
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 | 0.000007 |
Odds Ratio | 1.61 [1.31-1.97] |