rs5941047
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5941047(C;C) |
| Make rs5941047(C;T) |
| Make rs5941047(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 92176386 |
| Gene | PCDH11X |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5941047 |
| dbSNP (classic) | rs5941047 |
| ClinGen | rs5941047 |
| ebi | rs5941047 |
| HLI | rs5941047 |
| Exac | rs5941047 |
| Gnomad | rs5941047 |
| Varsome | rs5941047 |
| LitVar | rs5941047 |
| Map | rs5941047 |
| PheGenI | rs5941047 |
| Biobank | rs5941047 |
| 1000 genomes | rs5941047 |
| hgdp | rs5941047 |
| ensembl | rs5941047 |
| geneview | rs5941047 |
| scholar | rs5941047 |
| rs5941047 | |
| pharmgkb | rs5941047 |
| gwascentral | rs5941047 |
| openSNP | rs5941047 |
| 23andMe | rs5941047 |
| SNPshot | rs5941047 |
| SNPdbe | rs5941047 |
| MSV3d | rs5941047 |
| GWAS Ctlg | rs5941047 |
| GMAF | 0.4849 |
| 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.
