rs199962136
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs199962136(A;A) |
| Make rs199962136(A;G) |
| Make rs199962136(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 119052704 |
| Gene | HYOU1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199962136 |
| dbSNP (classic) | rs199962136 |
| ClinGen | rs199962136 |
| ebi | rs199962136 |
| HLI | rs199962136 |
| Exac | rs199962136 |
| Gnomad | rs199962136 |
| Varsome | rs199962136 |
| LitVar | rs199962136 |
| Map | rs199962136 |
| PheGenI | rs199962136 |
| Biobank | rs199962136 |
| 1000 genomes | rs199962136 |
| hgdp | rs199962136 |
| ensembl | rs199962136 |
| geneview | rs199962136 |
| scholar | rs199962136 |
| rs199962136 | |
| pharmgkb | rs199962136 |
| gwascentral | rs199962136 |
| openSNP | rs199962136 |
| 23andMe | rs199962136 |
| SNPshot | rs199962136 |
| SNPdbe | rs199962136 |
| MSV3d | rs199962136 |
| GWAS Ctlg | rs199962136 |
| Max Magnitude | 0 |
[PMID 27120077
] Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare variants speculated to have an impact (positive or negative; see publication for specific SNP details) on risk for bipolar disorder. The analysis of many more patients is likely to be required to confirm or refute this association.
