rs267607591
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs267607591(A;A) |
| Make rs267607591(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 156135274 |
| Gene | LMNA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs267607591 |
| dbSNP (classic) | rs267607591 |
| ClinGen | rs267607591 |
| ebi | rs267607591 |
| HLI | rs267607591 |
| Exac | rs267607591 |
| Gnomad | rs267607591 |
| Varsome | rs267607591 |
| LitVar | rs267607591 |
| Map | rs267607591 |
| PheGenI | rs267607591 |
| Biobank | rs267607591 |
| 1000 genomes | rs267607591 |
| hgdp | rs267607591 |
| ensembl | rs267607591 |
| geneview | rs267607591 |
| scholar | rs267607591 |
| rs267607591 | |
| pharmgkb | rs267607591 |
| gwascentral | rs267607591 |
| openSNP | rs267607591 |
| 23andMe | rs267607591 |
| SNPshot | rs267607591 |
| SNPdbe | rs267607591 |
| MSV3d | rs267607591 |
| GWAS Ctlg | rs267607591 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs267607591(A;A) |
| Alt | rs267607591(A;A) |
| Reference | Rs267607591(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided Lipodystrophy |
| Variation | info |
| Gene | LMNA |
| CLNDBN | not provided Lipodystrophy |
| Reversed | 0 |
| HGVS | NC_000001.10:g.156105065G>A |
| CLNSRC | ClinVar Epithelial Biology University of Chicago |
| CLNACC | RCV000057481.1, RCV000146262.1, |
