rs371709824
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs371709824(G;G) |
| Make rs371709824(G;T) |
| Make rs371709824(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 4 |
| Position | 786524 |
| Gene | CPLX1, LOC105374339 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs371709824 |
| dbSNP (classic) | rs371709824 |
| ClinGen | rs371709824 |
| ebi | rs371709824 |
| HLI | rs371709824 |
| Exac | rs371709824 |
| Gnomad | rs371709824 |
| Varsome | rs371709824 |
| LitVar | rs371709824 |
| Map | rs371709824 |
| PheGenI | rs371709824 |
| Biobank | rs371709824 |
| 1000 genomes | rs371709824 |
| hgdp | rs371709824 |
| ensembl | rs371709824 |
| geneview | rs371709824 |
| scholar | rs371709824 |
| rs371709824 | |
| pharmgkb | rs371709824 |
| gwascentral | rs371709824 |
| openSNP | rs371709824 |
| 23andMe | rs371709824 |
| SNPshot | rs371709824 |
| SNPdbe | rs371709824 |
| MSV3d | rs371709824 |
| GWAS Ctlg | rs371709824 |
| Max Magnitude | 0 |
aka NM_006651.3(CPLX1):c.382C>A or (p.Leu128Met)
OMIM pathogenic variant
