rs72624951
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common/normal |
| Make rs72624951(A;A) |
| Make rs72624951(A;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 7 |
| Position | 128403649 |
| Gene | IMPDH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs72624951 |
| dbSNP (classic) | rs72624951 |
| ClinGen | rs72624951 |
| ebi | rs72624951 |
| HLI | rs72624951 |
| Exac | rs72624951 |
| Gnomad | rs72624951 |
| Varsome | rs72624951 |
| LitVar | rs72624951 |
| Map | rs72624951 |
| PheGenI | rs72624951 |
| Biobank | rs72624951 |
| 1000 genomes | rs72624951 |
| hgdp | rs72624951 |
| ensembl | rs72624951 |
| geneview | rs72624951 |
| scholar | rs72624951 |
| rs72624951 | |
| pharmgkb | rs72624951 |
| gwascentral | rs72624951 |
| openSNP | rs72624951 |
| 23andMe | rs72624951 |
| SNPshot | rs72624951 |
| SNPdbe | rs72624951 |
| MSV3d | rs72624951 |
| GWAS Ctlg | rs72624951 |
| Max Magnitude | 0 |
Non-coding variant assessed as part of Blueprint Genetics Retinal dystrophy (266 gene) panel.
