rs59332535
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs59332535(A;A) |
| Make rs59332535(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 1 |
| Position | 156134911 |
| Gene | LMNA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs59332535 |
| dbSNP (classic) | rs59332535 |
| ClinGen | rs59332535 |
| ebi | rs59332535 |
| HLI | rs59332535 |
| Exac | rs59332535 |
| Gnomad | rs59332535 |
| Varsome | rs59332535 |
| LitVar | rs59332535 |
| Map | rs59332535 |
| PheGenI | rs59332535 |
| Biobank | rs59332535 |
| 1000 genomes | rs59332535 |
| hgdp | rs59332535 |
| ensembl | rs59332535 |
| geneview | rs59332535 |
| scholar | rs59332535 |
| rs59332535 | |
| pharmgkb | rs59332535 |
| gwascentral | rs59332535 |
| openSNP | rs59332535 |
| 23andMe | rs59332535 |
| SNPshot | rs59332535 |
| SNPdbe | rs59332535 |
| MSV3d | rs59332535 |
| GWAS Ctlg | rs59332535 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs59332535(A;A) |
| Alt | rs59332535(A;A) |
| Reference | Rs59332535(G;G) |
| Significance | Pathogenic |
| Disease | not provided Benign scapuloperoneal muscular dystrophy with cardiomyopathy |
| Variation | info |
| Gene | LMNA |
| CLNDBN | not provided Benign scapuloperoneal muscular dystrophy with cardiomyopathy |
| Reversed | 0 |
| HGVS | NC_000001.10:g.156104702G>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000057453.1, RCV000201012.2, |
