rs6563386
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6563386(C;C) |
| Make rs6563386(C;G) |
| Make rs6563386(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 13 |
| Position | 36202894 |
| Gene | CCDC169-SOHLH2, SOHLH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6563386 |
| dbSNP (classic) | rs6563386 |
| ClinGen | rs6563386 |
| ebi | rs6563386 |
| HLI | rs6563386 |
| Exac | rs6563386 |
| Gnomad | rs6563386 |
| Varsome | rs6563386 |
| LitVar | rs6563386 |
| Map | rs6563386 |
| PheGenI | rs6563386 |
| Biobank | rs6563386 |
| 1000 genomes | rs6563386 |
| hgdp | rs6563386 |
| ensembl | rs6563386 |
| geneview | rs6563386 |
| scholar | rs6563386 |
| rs6563386 | |
| pharmgkb | rs6563386 |
| gwascentral | rs6563386 |
| openSNP | rs6563386 |
| 23andMe | rs6563386 |
| SNPshot | rs6563386 |
| SNPdbe | rs6563386 |
| MSV3d | rs6563386 |
| GWAS Ctlg | rs6563386 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25463635] Association of genetic variants in SOHLH1 and SOHLH2 with non-obstructive azoospermia risk in the Chinese population
