rs41264871
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs41264871(A;G) |
| Make rs41264871(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 205066599 |
| Gene | CNTN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41264871 |
| dbSNP (classic) | rs41264871 |
| ClinGen | rs41264871 |
| ebi | rs41264871 |
| HLI | rs41264871 |
| Exac | rs41264871 |
| Gnomad | rs41264871 |
| Varsome | rs41264871 |
| LitVar | rs41264871 |
| Map | rs41264871 |
| PheGenI | rs41264871 |
| Biobank | rs41264871 |
| 1000 genomes | rs41264871 |
| hgdp | rs41264871 |
| ensembl | rs41264871 |
| geneview | rs41264871 |
| scholar | rs41264871 |
| rs41264871 | |
| pharmgkb | rs41264871 |
| gwascentral | rs41264871 |
| openSNP | rs41264871 |
| 23andMe | rs41264871 |
| SNPshot | rs41264871 |
| SNPdbe | rs41264871 |
| MSV3d | rs41264871 |
| GWAS Ctlg | rs41264871 |
| GMAF | 0.006887 |
| Max Magnitude | 0 |
[PMID 22462668] Single-nucleotide polymorphism of transient axonal glycoprotein-1 and its correlation with clinical features and prognosis in chronic inflammatory demyelinating polyneuropathy
