rs375554612
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs375554612(-;-) |
| Make rs375554612(-;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 13 |
| Position | 108209365 |
| Gene | LIG4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs375554612 |
| dbSNP (classic) | rs375554612 |
| ClinGen | rs375554612 |
| ebi | rs375554612 |
| HLI | rs375554612 |
| Exac | rs375554612 |
| Gnomad | rs375554612 |
| Varsome | rs375554612 |
| LitVar | rs375554612 |
| Map | rs375554612 |
| PheGenI | rs375554612 |
| Biobank | rs375554612 |
| 1000 genomes | rs375554612 |
| hgdp | rs375554612 |
| ensembl | rs375554612 |
| geneview | rs375554612 |
| scholar | rs375554612 |
| rs375554612 | |
| pharmgkb | rs375554612 |
| gwascentral | rs375554612 |
| openSNP | rs375554612 |
| 23andMe | rs375554612 |
| SNPshot | rs375554612 |
| SNPdbe | rs375554612 |
| MSV3d | rs375554612 |
| GWAS Ctlg | rs375554612 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs375554612(-;-) |
| Alt | rs375554612(-;-) |
| Reference | Rs375554612(T;T) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | LIG4 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000013.10:g.108861713delT |
| CLNSRC | |
| CLNACC | RCV000480290.1, |
