rs6031252
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs6031252(A;A) |
Make rs6031252(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 43945182 |
Gene | TOX2 |
is a | snp |
is | mentioned by |
dbSNP | rs6031252 |
dbSNP (classic) | rs6031252 |
ClinGen | rs6031252 |
ebi | rs6031252 |
HLI | rs6031252 |
Exac | rs6031252 |
Gnomad | rs6031252 |
Varsome | rs6031252 |
LitVar | rs6031252 |
Map | rs6031252 |
PheGenI | rs6031252 |
Biobank | rs6031252 |
1000 genomes | rs6031252 |
hgdp | rs6031252 |
ensembl | rs6031252 |
geneview | rs6031252 |
scholar | rs6031252 |
rs6031252 | |
pharmgkb | rs6031252 |
gwascentral | rs6031252 |
openSNP | rs6031252 |
23andMe | rs6031252 |
SNPshot | rs6031252 |
SNPdbe | rs6031252 |
MSV3d | rs6031252 |
GWAS Ctlg | rs6031252 |
GMAF | 0.1818 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20585324![]() |
Trait | Conduct disorder (symptom count) |
Title | Genome-wide association study of conduct disorder symptomatology |
Risk Allele | |
P-val | 0.000006 |
Odds Ratio | 0.11 [NR] unit decrease |