rs758539748
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs758539748(A;A) |
| Make rs758539748(A;G) |
| Make rs758539748(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 9 |
| Position | 135503655 |
| Gene | LOC101928525, MRPS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs758539748 |
| dbSNP (classic) | rs758539748 |
| ClinGen | rs758539748 |
| ebi | rs758539748 |
| HLI | rs758539748 |
| Exac | rs758539748 |
| Gnomad | rs758539748 |
| Varsome | rs758539748 |
| LitVar | rs758539748 |
| Map | rs758539748 |
| PheGenI | rs758539748 |
| Biobank | rs758539748 |
| 1000 genomes | rs758539748 |
| hgdp | rs758539748 |
| ensembl | rs758539748 |
| geneview | rs758539748 |
| scholar | rs758539748 |
| rs758539748 | |
| pharmgkb | rs758539748 |
| gwascentral | rs758539748 |
| openSNP | rs758539748 |
| 23andMe | rs758539748 |
| SNPshot | rs758539748 |
| SNPdbe | rs758539748 |
| MSV3d | rs758539748 |
| GWAS Ctlg | rs758539748 |
| Max Magnitude | 0 |
aka NM_016034.4(MRPS2):c.413G>A or (p.Arg138His)
OMIM pathogenic variant
