rs878853351
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs878853351(A;A) |
| Make rs878853351(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 4 |
| Position | 154744799 |
| Gene | LRAT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs878853351 |
| dbSNP (classic) | rs878853351 |
| ClinGen | rs878853351 |
| ebi | rs878853351 |
| HLI | rs878853351 |
| Exac | rs878853351 |
| Gnomad | rs878853351 |
| Varsome | rs878853351 |
| LitVar | rs878853351 |
| Map | rs878853351 |
| PheGenI | rs878853351 |
| Biobank | rs878853351 |
| 1000 genomes | rs878853351 |
| hgdp | rs878853351 |
| ensembl | rs878853351 |
| geneview | rs878853351 |
| scholar | rs878853351 |
| rs878853351 | |
| pharmgkb | rs878853351 |
| gwascentral | rs878853351 |
| openSNP | rs878853351 |
| 23andMe | rs878853351 |
| SNPshot | rs878853351 |
| SNPdbe | rs878853351 |
| MSV3d | rs878853351 |
| GWAS Ctlg | rs878853351 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs878853351(A;A) |
| Alt | rs878853351(A;A) |
| Reference | Rs878853351(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Retinal dystrophy |
| Variation | info |
| Gene | LRAT |
| CLNDBN | Retinal dystrophy |
| Reversed | 0 |
| HGVS | NC_000004.11:g.155665951G>A |
| CLNSRC | |
| CLNACC | RCV000225673.1, |
