rs773586710
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs773586710(-;-) |
| Make rs773586710(-;G) |
| Make rs773586710(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 15 |
| Position | 23645747 |
| Gene | MAGEL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs773586710 |
| dbSNP (classic) | rs773586710 |
| ClinGen | rs773586710 |
| ebi | rs773586710 |
| HLI | rs773586710 |
| Exac | rs773586710 |
| Gnomad | rs773586710 |
| Varsome | rs773586710 |
| LitVar | rs773586710 |
| Map | rs773586710 |
| PheGenI | rs773586710 |
| Biobank | rs773586710 |
| 1000 genomes | rs773586710 |
| hgdp | rs773586710 |
| ensembl | rs773586710 |
| geneview | rs773586710 |
| scholar | rs773586710 |
| rs773586710 | |
| pharmgkb | rs773586710 |
| gwascentral | rs773586710 |
| openSNP | rs773586710 |
| 23andMe | rs773586710 |
| SNPshot | rs773586710 |
| SNPdbe | rs773586710 |
| MSV3d | rs773586710 |
| GWAS Ctlg | rs773586710 |
| Max Magnitude | 0 |
aka NM_019066.4(MAGEL2):c.1996delC or (p.Gln666Serfs)
OMIM pathogenic variant
