rs7879933
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs7879933(A;A) |
| Make rs7879933(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 119583024 |
| Gene | UBE2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7879933 |
| dbSNP (classic) | rs7879933 |
| ClinGen | rs7879933 |
| ebi | rs7879933 |
| HLI | rs7879933 |
| Exac | rs7879933 |
| Gnomad | rs7879933 |
| Varsome | rs7879933 |
| LitVar | rs7879933 |
| Map | rs7879933 |
| PheGenI | rs7879933 |
| Biobank | rs7879933 |
| 1000 genomes | rs7879933 |
| hgdp | rs7879933 |
| ensembl | rs7879933 |
| geneview | rs7879933 |
| scholar | rs7879933 |
| rs7879933 | |
| pharmgkb | rs7879933 |
| gwascentral | rs7879933 |
| openSNP | rs7879933 |
| 23andMe | rs7879933 |
| SNPshot | rs7879933 |
| SNPdbe | rs7879933 |
| MSV3d | rs7879933 |
| GWAS Ctlg | rs7879933 |
| GMAF | 0.04414 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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-10 |
| Odds Ratio | NR NR |
