rs142534126
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs142534126(C;T) |
| Make rs142534126(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 4 |
| Position | 113345961 |
| Gene | ANK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs142534126 |
| dbSNP (classic) | rs142534126 |
| ClinGen | rs142534126 |
| ebi | rs142534126 |
| HLI | rs142534126 |
| Exac | rs142534126 |
| Gnomad | rs142534126 |
| Varsome | rs142534126 |
| LitVar | rs142534126 |
| Map | rs142534126 |
| PheGenI | rs142534126 |
| Biobank | rs142534126 |
| 1000 genomes | rs142534126 |
| hgdp | rs142534126 |
| ensembl | rs142534126 |
| geneview | rs142534126 |
| scholar | rs142534126 |
| rs142534126 | |
| pharmgkb | rs142534126 |
| gwascentral | rs142534126 |
| openSNP | rs142534126 |
| 23andMe | rs142534126 |
| SNPshot | rs142534126 |
| SNPdbe | rs142534126 |
| MSV3d | rs142534126 |
| GWAS Ctlg | rs142534126 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs142534126(T;T) |
| Alt | rs142534126(T;T) |
| Reference | Rs142534126(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided Cardiovascular phenotype |
| Variation | info |
| Gene | ANK2 |
| CLNDBN | not provided Cardiovascular phenotype |
| Reversed | 0 |
| HGVS | NC_000004.11:g.114267117C>T |
| CLNSRC | |
| CLNACC | RCV000170701.3, RCV000250831.1, |
