rs9834692
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9834692(C;C) |
| Make rs9834692(C;T) |
| Make rs9834692(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 87446400 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9834692 |
| dbSNP (classic) | rs9834692 |
| ClinGen | rs9834692 |
| ebi | rs9834692 |
| HLI | rs9834692 |
| Exac | rs9834692 |
| Gnomad | rs9834692 |
| Varsome | rs9834692 |
| LitVar | rs9834692 |
| Map | rs9834692 |
| PheGenI | rs9834692 |
| Biobank | rs9834692 |
| 1000 genomes | rs9834692 |
| hgdp | rs9834692 |
| ensembl | rs9834692 |
| geneview | rs9834692 |
| scholar | rs9834692 |
| rs9834692 | |
| pharmgkb | rs9834692 |
| gwascentral | rs9834692 |
| openSNP | rs9834692 |
| 23andMe | rs9834692 |
| SNPshot | rs9834692 |
| SNPdbe | rs9834692 |
| MSV3d | rs9834692 |
| GWAS Ctlg | rs9834692 |
| GMAF | 0.1281 |
| 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 | 3E-9 |
| Odds Ratio | NR NR |
