rs10569304
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10569304(-;-) |
| Make rs10569304(-;GCC) |
| Make rs10569304(GCC;GCC) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 105529713 |
| Gene | TMEM121 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10569304 |
| dbSNP (classic) | rs10569304 |
| ClinGen | rs10569304 |
| ebi | rs10569304 |
| HLI | rs10569304 |
| Exac | rs10569304 |
| Gnomad | rs10569304 |
| Varsome | rs10569304 |
| LitVar | rs10569304 |
| Map | rs10569304 |
| PheGenI | rs10569304 |
| Biobank | rs10569304 |
| 1000 genomes | rs10569304 |
| hgdp | rs10569304 |
| ensembl | rs10569304 |
| geneview | rs10569304 |
| scholar | rs10569304 |
| rs10569304 | |
| pharmgkb | rs10569304 |
| gwascentral | rs10569304 |
| openSNP | rs10569304 |
| 23andMe | rs10569304 |
| SNPshot | rs10569304 |
| SNPdbe | rs10569304 |
| MSV3d | rs10569304 |
| GWAS Ctlg | rs10569304 |
| GMAF | 0.3912 |
| Max Magnitude | 0 |
[PMID 20714865] Association between SNP rs10569304 on the second expressed region of hole gene and the congenital heart disease
