rs375681722
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs375681722(C;T) |
| Make rs375681722(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 11 |
| Position | 78702289 |
| Gene | TENM4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs375681722 |
| dbSNP (classic) | rs375681722 |
| ClinGen | rs375681722 |
| ebi | rs375681722 |
| HLI | rs375681722 |
| Exac | rs375681722 |
| Gnomad | rs375681722 |
| Varsome | rs375681722 |
| LitVar | rs375681722 |
| Map | rs375681722 |
| PheGenI | rs375681722 |
| Biobank | rs375681722 |
| 1000 genomes | rs375681722 |
| hgdp | rs375681722 |
| ensembl | rs375681722 |
| geneview | rs375681722 |
| scholar | rs375681722 |
| rs375681722 | |
| pharmgkb | rs375681722 |
| gwascentral | rs375681722 |
| openSNP | rs375681722 |
| 23andMe | rs375681722 |
| SNPshot | rs375681722 |
| SNPdbe | rs375681722 |
| MSV3d | rs375681722 |
| GWAS Ctlg | rs375681722 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs375681722(T;T) |
| Alt | rs375681722(T;T) |
| Reference | Rs375681722(C;C) |
| Significance | Pathogenic |
| Disease | Tremor |
| Variation | info |
| Gene | TENM4 |
| CLNDBN | Tremor, hereditary essential, 5 |
| Reversed | 0 |
| HGVS | NC_000011.9:g.78413334C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000203527.1, |
