rs753851892
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs753851892(A;A) |
| Make rs753851892(A;G) |
| Make rs753851892(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 6 |
| Position | 131858748 |
| Gene | ENPP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs753851892 |
| dbSNP (classic) | rs753851892 |
| ClinGen | rs753851892 |
| ebi | rs753851892 |
| HLI | rs753851892 |
| Exac | rs753851892 |
| Gnomad | rs753851892 |
| Varsome | rs753851892 |
| LitVar | rs753851892 |
| Map | rs753851892 |
| PheGenI | rs753851892 |
| Biobank | rs753851892 |
| 1000 genomes | rs753851892 |
| hgdp | rs753851892 |
| ensembl | rs753851892 |
| geneview | rs753851892 |
| scholar | rs753851892 |
| rs753851892 | |
| pharmgkb | rs753851892 |
| gwascentral | rs753851892 |
| openSNP | rs753851892 |
| 23andMe | rs753851892 |
| SNPshot | rs753851892 |
| SNPdbe | rs753851892 |
| MSV3d | rs753851892 |
| GWAS Ctlg | rs753851892 |
| Max Magnitude | 0 |
aka NM_006208.2(ENPP1):c.795+1G>A
OMIM pathogenic variant
