rs4568761
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4568761(C;C) |
| Make rs4568761(C;T) |
| Make rs4568761(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 92184068 |
| Gene | PCDH11X |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4568761 |
| dbSNP (classic) | rs4568761 |
| ClinGen | rs4568761 |
| ebi | rs4568761 |
| HLI | rs4568761 |
| Exac | rs4568761 |
| Gnomad | rs4568761 |
| Varsome | rs4568761 |
| LitVar | rs4568761 |
| Map | rs4568761 |
| PheGenI | rs4568761 |
| Biobank | rs4568761 |
| 1000 genomes | rs4568761 |
| hgdp | rs4568761 |
| ensembl | rs4568761 |
| geneview | rs4568761 |
| scholar | rs4568761 |
| rs4568761 | |
| pharmgkb | rs4568761 |
| gwascentral | rs4568761 |
| openSNP | rs4568761 |
| 23andMe | rs4568761 |
| SNPshot | rs4568761 |
| SNPdbe | rs4568761 |
| MSV3d | rs4568761 |
| GWAS Ctlg | rs4568761 |
| GMAF | 0.3077 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20523261
] PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility
[PMID 19136949] Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.
