rs2107856
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2107856(A;A) |
| Make rs2107856(A;C) |
| Make rs2107856(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 147491593 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2107856 |
| dbSNP (classic) | rs2107856 |
| ClinGen | rs2107856 |
| ebi | rs2107856 |
| HLI | rs2107856 |
| Exac | rs2107856 |
| Gnomad | rs2107856 |
| Varsome | rs2107856 |
| LitVar | rs2107856 |
| Map | rs2107856 |
| PheGenI | rs2107856 |
| Biobank | rs2107856 |
| 1000 genomes | rs2107856 |
| hgdp | rs2107856 |
| ensembl | rs2107856 |
| geneview | rs2107856 |
| scholar | rs2107856 |
| rs2107856 | |
| pharmgkb | rs2107856 |
| gwascentral | rs2107856 |
| openSNP | rs2107856 |
| 23andMe | rs2107856 |
| SNPshot | rs2107856 |
| SNPdbe | rs2107856 |
| MSV3d | rs2107856 |
| GWAS Ctlg | rs2107856 |
| GMAF | 0.3287 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 20808326
] Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome
