rs141191660
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common/normal |
| (A;G) | 3 | Carrier of progressive myoclonus epilepsy allele |
| Make rs141191660(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 7 |
| Position | 66639189 |
| Gene | KCTD7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141191660 |
| dbSNP (classic) | rs141191660 |
| ClinGen | rs141191660 |
| ebi | rs141191660 |
| HLI | rs141191660 |
| Exac | rs141191660 |
| Gnomad | rs141191660 |
| Varsome | rs141191660 |
| LitVar | rs141191660 |
| Map | rs141191660 |
| PheGenI | rs141191660 |
| Biobank | rs141191660 |
| 1000 genomes | rs141191660 |
| hgdp | rs141191660 |
| ensembl | rs141191660 |
| geneview | rs141191660 |
| scholar | rs141191660 |
| rs141191660 | |
| pharmgkb | rs141191660 |
| gwascentral | rs141191660 |
| openSNP | rs141191660 |
| 23andMe | rs141191660 |
| SNPshot | rs141191660 |
| SNPdbe | rs141191660 |
| MSV3d | rs141191660 |
| GWAS Ctlg | rs141191660 |
| Max Magnitude | 3 |
