rs35555197
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs35555197(A;A) |
| Make rs35555197(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 6 |
| Position | 107245583 |
| Gene | PDSS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35555197 |
| dbSNP (classic) | rs35555197 |
| ClinGen | rs35555197 |
| ebi | rs35555197 |
| HLI | rs35555197 |
| Exac | rs35555197 |
| Gnomad | rs35555197 |
| Varsome | rs35555197 |
| LitVar | rs35555197 |
| Map | rs35555197 |
| PheGenI | rs35555197 |
| Biobank | rs35555197 |
| 1000 genomes | rs35555197 |
| hgdp | rs35555197 |
| ensembl | rs35555197 |
| geneview | rs35555197 |
| scholar | rs35555197 |
| rs35555197 | |
| pharmgkb | rs35555197 |
| gwascentral | rs35555197 |
| openSNP | rs35555197 |
| 23andMe | rs35555197 |
| SNPshot | rs35555197 |
| SNPdbe | rs35555197 |
| MSV3d | rs35555197 |
| GWAS Ctlg | rs35555197 |
| 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 | rs35555197(A;A) |
| Alt | rs35555197(A;A) |
| Reference | Rs35555197(G;G) |
| Significance | Unknown |
| Disease | not specified Coenzyme Q10 deficiency |
| Variation | info |
| Gene | PDSS2 |
| CLNDBN | not specified Coenzyme Q10 deficiency, primary |
| Reversed | 1 |
| HGVS | NC_000006.11:g.107566787C>T |
| CLNSRC | |
| CLNACC | RCV000197521.3, RCV000311116.1, |
