rs4434872
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4434872(C;C) |
Make rs4434872(C;T) |
Make rs4434872(T;T) |
Reference | GRCh37.p5 37.3/137 |
Chromosome | 1 |
Position | 153801800 |
Gene | LOC105371448 |
is a | snp |
is | mentioned by |
dbSNP | rs4434872 |
dbSNP (classic) | rs4434872 |
ClinGen | rs4434872 |
ebi | rs4434872 |
HLI | rs4434872 |
Exac | rs4434872 |
Gnomad | rs4434872 |
Varsome | rs4434872 |
LitVar | rs4434872 |
Map | rs4434872 |
PheGenI | rs4434872 |
Biobank | rs4434872 |
1000 genomes | rs4434872 |
hgdp | rs4434872 |
ensembl | rs4434872 |
geneview | rs4434872 |
scholar | rs4434872 |
rs4434872 | |
pharmgkb | rs4434872 |
gwascentral | rs4434872 |
openSNP | rs4434872 |
23andMe | rs4434872 |
SNPshot | rs4434872 |
SNPdbe | rs4434872 |
MSV3d | rs4434872 |
GWAS Ctlg | rs4434872 |
GMAF | 0.3411 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 0.08 [NR] unit increase |
[PMID 18505370] Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women.