rs375954692
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs375954692(C;C) |
| Make rs375954692(C;T) |
| Make rs375954692(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 1250169 |
| Gene | MUC5B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs375954692 |
| dbSNP (classic) | rs375954692 |
| ClinGen | rs375954692 |
| ebi | rs375954692 |
| HLI | rs375954692 |
| Exac | rs375954692 |
| Gnomad | rs375954692 |
| Varsome | rs375954692 |
| LitVar | rs375954692 |
| Map | rs375954692 |
| PheGenI | rs375954692 |
| Biobank | rs375954692 |
| 1000 genomes | rs375954692 |
| hgdp | rs375954692 |
| ensembl | rs375954692 |
| geneview | rs375954692 |
| scholar | rs375954692 |
| rs375954692 | |
| pharmgkb | rs375954692 |
| gwascentral | rs375954692 |
| openSNP | rs375954692 |
| 23andMe | rs375954692 |
| SNPshot | rs375954692 |
| SNPdbe | rs375954692 |
| MSV3d | rs375954692 |
| GWAS Ctlg | rs375954692 |
| 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.
