rs144288263
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs144288263(A;A) |
| Make rs144288263(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 8 |
| Position | 27787965 |
| Gene | ESCO2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs144288263 |
| dbSNP (classic) | rs144288263 |
| ClinGen | rs144288263 |
| ebi | rs144288263 |
| HLI | rs144288263 |
| Exac | rs144288263 |
| Gnomad | rs144288263 |
| Varsome | rs144288263 |
| LitVar | rs144288263 |
| Map | rs144288263 |
| PheGenI | rs144288263 |
| Biobank | rs144288263 |
| 1000 genomes | rs144288263 |
| hgdp | rs144288263 |
| ensembl | rs144288263 |
| geneview | rs144288263 |
| scholar | rs144288263 |
| rs144288263 | |
| pharmgkb | rs144288263 |
| gwascentral | rs144288263 |
| openSNP | rs144288263 |
| 23andMe | rs144288263 |
| SNPshot | rs144288263 |
| SNPdbe | rs144288263 |
| MSV3d | rs144288263 |
| GWAS Ctlg | rs144288263 |
| 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.
| ClinVar | |
|---|---|
| Risk | rs144288263(A;A) |
| Alt | rs144288263(A;A) |
| Reference | Rs144288263(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | ESCO2 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000008.10:g.27645482G>A |
| CLNSRC | |
| CLNACC | RCV000395189.1, |
