rs776095655
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs776095655(A;A) |
| Make rs776095655(A;C) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 42927684 |
| Gene | SLC2A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs776095655 |
| dbSNP (classic) | rs776095655 |
| ClinGen | rs776095655 |
| ebi | rs776095655 |
| HLI | rs776095655 |
| Exac | rs776095655 |
| Gnomad | rs776095655 |
| Varsome | rs776095655 |
| LitVar | rs776095655 |
| Map | rs776095655 |
| PheGenI | rs776095655 |
| Biobank | rs776095655 |
| 1000 genomes | rs776095655 |
| hgdp | rs776095655 |
| ensembl | rs776095655 |
| geneview | rs776095655 |
| scholar | rs776095655 |
| rs776095655 | |
| pharmgkb | rs776095655 |
| gwascentral | rs776095655 |
| openSNP | rs776095655 |
| 23andMe | rs776095655 |
| SNPshot | rs776095655 |
| SNPdbe | rs776095655 |
| MSV3d | rs776095655 |
| GWAS Ctlg | rs776095655 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs776095655(A;A) rs776095655(T;T) |
| Alt | rs776095655(A;A) rs776095655(T;T) |
| Reference | Rs776095655(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SLC2A1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.43393355C>T |
| CLNSRC | |
| CLNACC | RCV000364606.1, |
