rs777367269
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs777367269(A;A) |
| Make rs777367269(A;G) |
| Make rs777367269(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 6 |
| Position | 131877024 |
| Gene | ENPP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs777367269 |
| dbSNP (classic) | rs777367269 |
| ClinGen | rs777367269 |
| ebi | rs777367269 |
| HLI | rs777367269 |
| Exac | rs777367269 |
| Gnomad | rs777367269 |
| Varsome | rs777367269 |
| LitVar | rs777367269 |
| Map | rs777367269 |
| PheGenI | rs777367269 |
| Biobank | rs777367269 |
| 1000 genomes | rs777367269 |
| hgdp | rs777367269 |
| ensembl | rs777367269 |
| geneview | rs777367269 |
| scholar | rs777367269 |
| rs777367269 | |
| pharmgkb | rs777367269 |
| gwascentral | rs777367269 |
| openSNP | rs777367269 |
| 23andMe | rs777367269 |
| SNPshot | rs777367269 |
| SNPdbe | rs777367269 |
| MSV3d | rs777367269 |
| GWAS Ctlg | rs777367269 |
| Max Magnitude | 0 |
aka NM_006208.2(ENPP1):c.1756G>A or (p.Gly586Arg)
OMIM pathogenic variant
