rs61889560
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs61889560(A;A) |
| Make rs61889560(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 68423568 |
| Gene | LRP5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61889560 |
| dbSNP (classic) | rs61889560 |
| ClinGen | rs61889560 |
| ebi | rs61889560 |
| HLI | rs61889560 |
| Exac | rs61889560 |
| Gnomad | rs61889560 |
| Varsome | rs61889560 |
| LitVar | rs61889560 |
| Map | rs61889560 |
| PheGenI | rs61889560 |
| Biobank | rs61889560 |
| 1000 genomes | rs61889560 |
| hgdp | rs61889560 |
| ensembl | rs61889560 |
| geneview | rs61889560 |
| scholar | rs61889560 |
| rs61889560 | |
| pharmgkb | rs61889560 |
| gwascentral | rs61889560 |
| openSNP | rs61889560 |
| 23andMe | rs61889560 |
| SNPshot | rs61889560 |
| SNPdbe | rs61889560 |
| MSV3d | rs61889560 |
| GWAS Ctlg | rs61889560 |
| 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 | rs61889560(A;A) rs61889560(T;T) |
| Alt | rs61889560(A;A) rs61889560(T;T) |
| Reference | Rs61889560(G;G) |
| Significance | Untested |
| Disease | Polycystic kidney disease not specified |
| Variation | info |
| Gene | LRP5 |
| CLNDBN | Polycystic kidney disease, adult type not specified |
| Reversed | 0 |
| HGVS | NC_000011.9:g.68191036G>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000162089.1, RCV000174732.2, |
