rs17024684
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17024684(C;C) |
| Make rs17024684(C;T) |
| Make rs17024684(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 3013563 |
| Gene | CNTN4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17024684 |
| dbSNP (classic) | rs17024684 |
| ClinGen | rs17024684 |
| ebi | rs17024684 |
| HLI | rs17024684 |
| Exac | rs17024684 |
| Gnomad | rs17024684 |
| Varsome | rs17024684 |
| LitVar | rs17024684 |
| Map | rs17024684 |
| PheGenI | rs17024684 |
| Biobank | rs17024684 |
| 1000 genomes | rs17024684 |
| hgdp | rs17024684 |
| ensembl | rs17024684 |
| geneview | rs17024684 |
| scholar | rs17024684 |
| rs17024684 | |
| pharmgkb | rs17024684 |
| gwascentral | rs17024684 |
| openSNP | rs17024684 |
| 23andMe | rs17024684 |
| SNPshot | rs17024684 |
| SNPdbe | rs17024684 |
| MSV3d | rs17024684 |
| GWAS Ctlg | rs17024684 |
| GMAF | 0.0877 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23471985 ]
|
| Trait | Brain connectivity |
| Title | Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity. |
| Risk Allele | |
| P-val | 2E-9 |
| Odds Ratio | NR NR |
