rs201076428
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs201076428(C;T) |
| Make rs201076428(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 7 |
| Position | 147639254 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201076428 |
| dbSNP (classic) | rs201076428 |
| ClinGen | rs201076428 |
| ebi | rs201076428 |
| HLI | rs201076428 |
| Exac | rs201076428 |
| Gnomad | rs201076428 |
| Varsome | rs201076428 |
| LitVar | rs201076428 |
| Map | rs201076428 |
| PheGenI | rs201076428 |
| Biobank | rs201076428 |
| 1000 genomes | rs201076428 |
| hgdp | rs201076428 |
| ensembl | rs201076428 |
| geneview | rs201076428 |
| scholar | rs201076428 |
| rs201076428 | |
| pharmgkb | rs201076428 |
| gwascentral | rs201076428 |
| openSNP | rs201076428 |
| 23andMe | rs201076428 |
| SNPshot | rs201076428 |
| SNPdbe | rs201076428 |
| MSV3d | rs201076428 |
| GWAS Ctlg | rs201076428 |
| Max Magnitude | 0 |
OMIM pathogenic variant
