rs1328626
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1328626(G;G) |
| Make rs1328626(G;T) |
| Make rs1328626(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 13 |
| Position | 36204635 |
| Gene | CCDC169-SOHLH2, SOHLH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1328626 |
| dbSNP (classic) | rs1328626 |
| ClinGen | rs1328626 |
| ebi | rs1328626 |
| HLI | rs1328626 |
| Exac | rs1328626 |
| Gnomad | rs1328626 |
| Varsome | rs1328626 |
| LitVar | rs1328626 |
| Map | rs1328626 |
| PheGenI | rs1328626 |
| Biobank | rs1328626 |
| 1000 genomes | rs1328626 |
| hgdp | rs1328626 |
| ensembl | rs1328626 |
| geneview | rs1328626 |
| scholar | rs1328626 |
| rs1328626 | |
| pharmgkb | rs1328626 |
| gwascentral | rs1328626 |
| openSNP | rs1328626 |
| 23andMe | rs1328626 |
| SNPshot | rs1328626 |
| SNPdbe | rs1328626 |
| MSV3d | rs1328626 |
| GWAS Ctlg | rs1328626 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25463635] Association of genetic variants in SOHLH1 and SOHLH2 with non-obstructive azoospermia risk in the Chinese population
