rs375836361
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs375836361(C;T) |
| Make rs375836361(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 2 |
| Position | 27497334 |
| Gene | GCKR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs375836361 |
| dbSNP (classic) | rs375836361 |
| ClinGen | rs375836361 |
| ebi | rs375836361 |
| HLI | rs375836361 |
| Exac | rs375836361 |
| Gnomad | rs375836361 |
| Varsome | rs375836361 |
| LitVar | rs375836361 |
| Map | rs375836361 |
| PheGenI | rs375836361 |
| Biobank | rs375836361 |
| 1000 genomes | rs375836361 |
| hgdp | rs375836361 |
| ensembl | rs375836361 |
| geneview | rs375836361 |
| scholar | rs375836361 |
| rs375836361 | |
| pharmgkb | rs375836361 |
| gwascentral | rs375836361 |
| openSNP | rs375836361 |
| 23andMe | rs375836361 |
| SNPshot | rs375836361 |
| SNPdbe | rs375836361 |
| MSV3d | rs375836361 |
| GWAS Ctlg | rs375836361 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs375836361(G;G) rs375836361(T;T) |
| Alt | rs375836361(G;G) rs375836361(T;T) |
| Reference | Rs375836361(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GCKR |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.27720201C>T |
| CLNSRC | |
| CLNACC | RCV000256099.1, |
