rs774359
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs774359(C;C) |
| Make rs774359(C;T) |
| Make rs774359(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 27561051 |
| Gene | C9orf72 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs774359 |
| dbSNP (classic) | rs774359 |
| ClinGen | rs774359 |
| ebi | rs774359 |
| HLI | rs774359 |
| Exac | rs774359 |
| Gnomad | rs774359 |
| Varsome | rs774359 |
| LitVar | rs774359 |
| Map | rs774359 |
| PheGenI | rs774359 |
| Biobank | rs774359 |
| 1000 genomes | rs774359 |
| hgdp | rs774359 |
| ensembl | rs774359 |
| geneview | rs774359 |
| scholar | rs774359 |
| rs774359 | |
| pharmgkb | rs774359 |
| gwascentral | rs774359 |
| openSNP | rs774359 |
| 23andMe | rs774359 |
| SNPshot | rs774359 |
| SNPdbe | rs774359 |
| MSV3d | rs774359 |
| GWAS Ctlg | rs774359 |
| GMAF | 0.1997 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19734901] |
| Trait | Amyotrophic lateral sclerosis |
| Title | Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis |
| Risk Allele | |
| P-val | 0.000003 |
| Odds Ratio | 1.19 [NR] |
[PMID 20423481
] Lack of replication of genetic predictors for the rheumatoid arthritis response to anti-TNF treatments: a prospective case-only study.
