rs766251466
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (GAG;GAG) | 0 | common in clinvar |
| Make rs766251466(-;-) |
| Make rs766251466(-;GAG) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 20 |
| Position | 3916956 |
| Gene | MIR103A2, PANK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs766251466 |
| dbSNP (classic) | rs766251466 |
| ClinGen | rs766251466 |
| ebi | rs766251466 |
| HLI | rs766251466 |
| Exac | rs766251466 |
| Gnomad | rs766251466 |
| Varsome | rs766251466 |
| LitVar | rs766251466 |
| Map | rs766251466 |
| PheGenI | rs766251466 |
| Biobank | rs766251466 |
| 1000 genomes | rs766251466 |
| hgdp | rs766251466 |
| ensembl | rs766251466 |
| geneview | rs766251466 |
| scholar | rs766251466 |
| rs766251466 | |
| pharmgkb | rs766251466 |
| gwascentral | rs766251466 |
| openSNP | rs766251466 |
| 23andMe | rs766251466 |
| SNPshot | rs766251466 |
| SNPdbe | rs766251466 |
| MSV3d | rs766251466 |
| GWAS Ctlg | rs766251466 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs766251466(-;-) |
| Alt | rs766251466(-;-) |
| Reference | Rs766251466(GAG;GAG) |
| Significance | Pathogenic |
| Disease | Pigmentary pallidal degeneration |
| Variation | info |
| Gene | MIR103A2 PANK2 |
| CLNDBN | Pigmentary pallidal degeneration |
| Reversed | 0 |
| HGVS | NC_000020.10:g.3897603_3897605delGAG |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000004822.2, |
