rs780606789
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs780606789(C;C) |
| Make rs780606789(C;T) |
| Make rs780606789(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 16 |
| Position | 31191546 |
| Gene | FUS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs780606789 |
| dbSNP (classic) | rs780606789 |
| ClinGen | rs780606789 |
| ebi | rs780606789 |
| HLI | rs780606789 |
| Exac | rs780606789 |
| Gnomad | rs780606789 |
| Varsome | rs780606789 |
| LitVar | rs780606789 |
| Map | rs780606789 |
| PheGenI | rs780606789 |
| Biobank | rs780606789 |
| 1000 genomes | rs780606789 |
| hgdp | rs780606789 |
| ensembl | rs780606789 |
| geneview | rs780606789 |
| scholar | rs780606789 |
| rs780606789 | |
| pharmgkb | rs780606789 |
| gwascentral | rs780606789 |
| openSNP | rs780606789 |
| 23andMe | rs780606789 |
| SNPshot | rs780606789 |
| SNPdbe | rs780606789 |
| MSV3d | rs780606789 |
| GWAS Ctlg | rs780606789 |
| Max Magnitude | 0 |
[PMID 27569544
] A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. This SNP maps to a position listed in Table S6 as a non-coding variant that their biocurators felt was convincingly associated with a Mendelian disease.
