rs183105855
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs183105855(C;C) |
| Make rs183105855(C;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 14 |
| Position | 87965582 |
| Gene | GALC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs183105855 |
| dbSNP (classic) | rs183105855 |
| ClinGen | rs183105855 |
| ebi | rs183105855 |
| HLI | rs183105855 |
| Exac | rs183105855 |
| Gnomad | rs183105855 |
| Varsome | rs183105855 |
| LitVar | rs183105855 |
| Map | rs183105855 |
| PheGenI | rs183105855 |
| Biobank | rs183105855 |
| 1000 genomes | rs183105855 |
| hgdp | rs183105855 |
| ensembl | rs183105855 |
| geneview | rs183105855 |
| scholar | rs183105855 |
| rs183105855 | |
| pharmgkb | rs183105855 |
| gwascentral | rs183105855 |
| openSNP | rs183105855 |
| 23andMe | rs183105855 |
| SNPshot | rs183105855 |
| SNPdbe | rs183105855 |
| MSV3d | rs183105855 |
| GWAS Ctlg | rs183105855 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs183105855(C;C) |
| Alt | rs183105855(C;C) |
| Reference | Rs183105855(T;T) |
| Significance | Other |
| Disease | not provided |
| Variation | info |
| Gene | GALC |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000014.8:g.88431926T>C |
| CLNSRC | |
| CLNACC | RCV000255537.1, |
