rs929867
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs929867(C;C) |
| Make rs929867(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 31180161 |
| Gene | FUS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs929867 |
| dbSNP (classic) | rs929867 |
| ClinGen | rs929867 |
| ebi | rs929867 |
| HLI | rs929867 |
| Exac | rs929867 |
| Gnomad | rs929867 |
| Varsome | rs929867 |
| LitVar | rs929867 |
| Map | rs929867 |
| PheGenI | rs929867 |
| Biobank | rs929867 |
| 1000 genomes | rs929867 |
| hgdp | rs929867 |
| ensembl | rs929867 |
| geneview | rs929867 |
| scholar | rs929867 |
| rs929867 | |
| pharmgkb | rs929867 |
| gwascentral | rs929867 |
| openSNP | rs929867 |
| 23andMe | rs929867 |
| SNPshot | rs929867 |
| SNPdbe | rs929867 |
| MSV3d | rs929867 |
| GWAS Ctlg | rs929867 |
| Max Magnitude | 0 |
Although based on a relatively small study, there's a strong association (odds ratios above 30) between the very rare (and neighboring) minor alleles of rs8056264 and rs929867 with common variable immunodeficiency (CVID) reported in [PMID 25678086
].
| ClinVar | |
|---|---|
| Risk | rs929867(C;C) |
| Alt | rs929867(C;C) |
| Reference | Rs929867(T;T) |
| Significance | Non-pathogenic |
| Disease | Amyotrophic Lateral Sclerosis |
| Variation | info |
| Gene | FUS |
| CLNDBN | Amyotrophic Lateral Sclerosis, Dominant |
| Reversed | 1 |
| HGVS | NC_000016.9:g.31191482A>G |
| CLNSRC | |
| CLNACC | RCV000307180.1, |
