rs534934297
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs534934297(A;G) |
| Make rs534934297(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 4 |
| Position | 113356942 |
| Gene | ANK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs534934297 |
| dbSNP (classic) | rs534934297 |
| ClinGen | rs534934297 |
| ebi | rs534934297 |
| HLI | rs534934297 |
| Exac | rs534934297 |
| Gnomad | rs534934297 |
| Varsome | rs534934297 |
| LitVar | rs534934297 |
| Map | rs534934297 |
| PheGenI | rs534934297 |
| Biobank | rs534934297 |
| 1000 genomes | rs534934297 |
| hgdp | rs534934297 |
| ensembl | rs534934297 |
| geneview | rs534934297 |
| scholar | rs534934297 |
| rs534934297 | |
| pharmgkb | rs534934297 |
| gwascentral | rs534934297 |
| openSNP | rs534934297 |
| 23andMe | rs534934297 |
| SNPshot | rs534934297 |
| SNPdbe | rs534934297 |
| MSV3d | rs534934297 |
| GWAS Ctlg | rs534934297 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs534934297(G;G) |
| Alt | rs534934297(G;G) |
| Reference | Rs534934297(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ANK2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000004.11:g.114278098A>G |
| CLNSRC | |
| CLNACC | RCV000171381.1, |
