rs2935183
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2935183(A;A) |
| Make rs2935183(A;C) |
| Make rs2935183(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 47530206 |
| Gene | NPEPPS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2935183 |
| dbSNP (classic) | rs2935183 |
| ClinGen | rs2935183 |
| ebi | rs2935183 |
| HLI | rs2935183 |
| Exac | rs2935183 |
| Gnomad | rs2935183 |
| Varsome | rs2935183 |
| LitVar | rs2935183 |
| Map | rs2935183 |
| PheGenI | rs2935183 |
| Biobank | rs2935183 |
| 1000 genomes | rs2935183 |
| hgdp | rs2935183 |
| ensembl | rs2935183 |
| geneview | rs2935183 |
| scholar | rs2935183 |
| rs2935183 | |
| pharmgkb | rs2935183 |
| gwascentral | rs2935183 |
| openSNP | rs2935183 |
| 23andMe | rs2935183 |
| SNPshot | rs2935183 |
| SNPdbe | rs2935183 |
| MSV3d | rs2935183 |
| GWAS Ctlg | rs2935183 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 24234648 ]
|
| Trait | Multiple sclerosis or amyotrophic lateral sclerosis |
| Title | No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. |
| Risk Allele | |
| P-val | 5E-7 |
| Odds Ratio | NR NR |
