rs537053537
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs537053537(C;C) |
| Make rs537053537(C;T) |
| Make rs537053537(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 19 |
| Position | 40374524 |
| Gene | PLD3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs537053537 |
| dbSNP (classic) | rs537053537 |
| ClinGen | rs537053537 |
| ebi | rs537053537 |
| HLI | rs537053537 |
| Exac | rs537053537 |
| Gnomad | rs537053537 |
| Varsome | rs537053537 |
| LitVar | rs537053537 |
| Map | rs537053537 |
| PheGenI | rs537053537 |
| Biobank | rs537053537 |
| 1000 genomes | rs537053537 |
| hgdp | rs537053537 |
| ensembl | rs537053537 |
| geneview | rs537053537 |
| scholar | rs537053537 |
| rs537053537 | |
| pharmgkb | rs537053537 |
| gwascentral | rs537053537 |
| openSNP | rs537053537 |
| 23andMe | rs537053537 |
| SNPshot | rs537053537 |
| SNPdbe | rs537053537 |
| MSV3d | rs537053537 |
| GWAS Ctlg | rs537053537 |
| Max Magnitude | 0 |
aka NM_012268.3(PLD3):c.923T>C or (p.Leu308Pro)
OMIM pathogenic variant
