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.
