rs12302829
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs12302829(A;G) |
Make rs12302829(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 5031318 |
Gene | FMR1NB |
is a | snp |
is | mentioned by |
dbSNP | rs12302829 |
dbSNP (classic) | rs12302829 |
ClinGen | rs12302829 |
ebi | rs12302829 |
HLI | rs12302829 |
Exac | rs12302829 |
Gnomad | rs12302829 |
Varsome | rs12302829 |
LitVar | rs12302829 |
Map | rs12302829 |
PheGenI | rs12302829 |
Biobank | rs12302829 |
1000 genomes | rs12302829 |
hgdp | rs12302829 |
ensembl | rs12302829 |
geneview | rs12302829 |
scholar | rs12302829 |
rs12302829 | |
pharmgkb | rs12302829 |
gwascentral | rs12302829 |
openSNP | rs12302829 |
23andMe | rs12302829 |
SNPshot | rs12302829 |
SNPdbe | rs12302829 |
MSV3d | rs12302829 |
GWAS Ctlg | rs12302829 |
GMAF | 0.0101 |
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 | 0.000008 |
Odds Ratio | 0.35 [NR] unit decrease |