rs869312740
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs869312740(G;G) |
| Make rs869312740(G;T) |
| Make rs869312740(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 22 |
| Position | 26026470 |
| Gene | MYO18B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs869312740 |
| dbSNP (classic) | rs869312740 |
| ClinGen | rs869312740 |
| ebi | rs869312740 |
| HLI | rs869312740 |
| Exac | rs869312740 |
| Gnomad | rs869312740 |
| Varsome | rs869312740 |
| LitVar | rs869312740 |
| Map | rs869312740 |
| PheGenI | rs869312740 |
| Biobank | rs869312740 |
| 1000 genomes | rs869312740 |
| hgdp | rs869312740 |
| ensembl | rs869312740 |
| geneview | rs869312740 |
| scholar | rs869312740 |
| rs869312740 | |
| pharmgkb | rs869312740 |
| gwascentral | rs869312740 |
| openSNP | rs869312740 |
| 23andMe | rs869312740 |
| SNPshot | rs869312740 |
| SNPdbe | rs869312740 |
| MSV3d | rs869312740 |
| GWAS Ctlg | rs869312740 |
| Max Magnitude | 0 |
aka NM_032608.6(MYO18B):c.6496G>T or (p.Glu2166Ter)
OMIM pathogenic variant
