rs10035961
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10035961(A;A) |
| Make rs10035961(A;C) |
| Make rs10035961(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 157603387 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10035961 |
| dbSNP (classic) | rs10035961 |
| ClinGen | rs10035961 |
| ebi | rs10035961 |
| HLI | rs10035961 |
| Exac | rs10035961 |
| Gnomad | rs10035961 |
| Varsome | rs10035961 |
| LitVar | rs10035961 |
| Map | rs10035961 |
| PheGenI | rs10035961 |
| Biobank | rs10035961 |
| 1000 genomes | rs10035961 |
| hgdp | rs10035961 |
| ensembl | rs10035961 |
| geneview | rs10035961 |
| scholar | rs10035961 |
| rs10035961 | |
| pharmgkb | rs10035961 |
| gwascentral | rs10035961 |
| openSNP | rs10035961 |
| 23andMe | rs10035961 |
| 23andMe all | rs10035961 |
| SNPshot | rs10035961 |
| SNPdbe | rs10035961 |
| MSV3d | rs10035961 |
| GWAS Ctlg | rs10035961 |
| GMAF | 0.3563 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 19319892
] A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees.
