rs55883237
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;G) | 5 | Left ventricular noncompaction possible (likely?) |
| (G;G) | 0 | common/normal |
| Make rs55883237(C;C) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 1 |
| Position | 228374584 |
| Gene | OBSCN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs55883237 |
| dbSNP (classic) | rs55883237 |
| ClinGen | rs55883237 |
| ebi | rs55883237 |
| HLI | rs55883237 |
| Exac | rs55883237 |
| Gnomad | rs55883237 |
| Varsome | rs55883237 |
| LitVar | rs55883237 |
| Map | rs55883237 |
| PheGenI | rs55883237 |
| Biobank | rs55883237 |
| 1000 genomes | rs55883237 |
| hgdp | rs55883237 |
| ensembl | rs55883237 |
| geneview | rs55883237 |
| scholar | rs55883237 |
| rs55883237 | |
| pharmgkb | rs55883237 |
| gwascentral | rs55883237 |
| openSNP | rs55883237 |
| 23andMe | rs55883237 |
| SNPshot | rs55883237 |
| SNPdbe | rs55883237 |
| MSV3d | rs55883237 |
| GWAS Ctlg | rs55883237 |
| Max Magnitude | 5 |
The rare minor allele of this OBSCN SNP is reported in 10.1016/j.jacc.2016.08.052 to be a variant leading to left ventricular noncompaction, acting in a dominant manner (i.e. in heterozygotes).
