rs761095873
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs761095873(-;-) |
| Make rs761095873(-;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 3 |
| Position | 158666381 |
| Gene | GFM1, LXN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs761095873 |
| dbSNP (classic) | rs761095873 |
| ClinGen | rs761095873 |
| ebi | rs761095873 |
| HLI | rs761095873 |
| Exac | rs761095873 |
| Gnomad | rs761095873 |
| Varsome | rs761095873 |
| LitVar | rs761095873 |
| Map | rs761095873 |
| PheGenI | rs761095873 |
| Biobank | rs761095873 |
| 1000 genomes | rs761095873 |
| hgdp | rs761095873 |
| ensembl | rs761095873 |
| geneview | rs761095873 |
| scholar | rs761095873 |
| rs761095873 | |
| pharmgkb | rs761095873 |
| gwascentral | rs761095873 |
| openSNP | rs761095873 |
| 23andMe | rs761095873 |
| SNPshot | rs761095873 |
| SNPdbe | rs761095873 |
| MSV3d | rs761095873 |
| GWAS Ctlg | rs761095873 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs761095873(-;-) |
| Alt | rs761095873(-;-) |
| Reference | Rs761095873(T;T) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GFM1 LXN |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000003.11:g.158384170delT |
| CLNSRC | |
| CLNACC | RCV000196892.1, |
