rs10800485
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10800485(C;C) |
| Make rs10800485(C;T) |
| Make rs10800485(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 169878005 |
| Gene | SCYL3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10800485 |
| dbSNP (classic) | rs10800485 |
| ClinGen | rs10800485 |
| ebi | rs10800485 |
| HLI | rs10800485 |
| Exac | rs10800485 |
| Gnomad | rs10800485 |
| Varsome | rs10800485 |
| LitVar | rs10800485 |
| Map | rs10800485 |
| PheGenI | rs10800485 |
| Biobank | rs10800485 |
| 1000 genomes | rs10800485 |
| hgdp | rs10800485 |
| ensembl | rs10800485 |
| geneview | rs10800485 |
| scholar | rs10800485 |
| rs10800485 | |
| pharmgkb | rs10800485 |
| gwascentral | rs10800485 |
| openSNP | rs10800485 |
| 23andMe | rs10800485 |
| SNPshot | rs10800485 |
| SNPdbe | rs10800485 |
| MSV3d | rs10800485 |
| GWAS Ctlg | rs10800485 |
| GMAF | 0.331 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 17357082
] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
