rs7721142
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7721142(C;C) |
| Make rs7721142(C;G) |
| Make rs7721142(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 157525400 |
| Gene | ADAM19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7721142 |
| dbSNP (classic) | rs7721142 |
| ClinGen | rs7721142 |
| ebi | rs7721142 |
| HLI | rs7721142 |
| Exac | rs7721142 |
| Gnomad | rs7721142 |
| Varsome | rs7721142 |
| LitVar | rs7721142 |
| Map | rs7721142 |
| PheGenI | rs7721142 |
| Biobank | rs7721142 |
| 1000 genomes | rs7721142 |
| hgdp | rs7721142 |
| ensembl | rs7721142 |
| geneview | rs7721142 |
| scholar | rs7721142 |
| rs7721142 | |
| pharmgkb | rs7721142 |
| gwascentral | rs7721142 |
| openSNP | rs7721142 |
| 23andMe | rs7721142 |
| SNPshot | rs7721142 |
| SNPdbe | rs7721142 |
| MSV3d | rs7721142 |
| GWAS Ctlg | rs7721142 |
| GMAF | 0.2998 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19319892
] A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees.
